Editing SDHD (section)

== Further reading ==
{{refbegin|33em}}
* {{cite journal | vauthors = Bayley JP, Weiss MM, Grimbergen A, van Brussel BT, Hes FJ, Jansen JC, Verhoef S, Devilee P, Corssmit EP, Vriends AH | title = Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients | journal = Endocrine-Related Cancer | volume = 16 | issue = 3 | pages = 929–37 | date = September 2009 | pmid = 19546167 | doi = 10.1677/ERC-09-0084 | doi-access = free }}
* {{cite journal | vauthors = Gaal J, Burnichon N, Korpershoek E, Roncelin I, Bertherat J, Plouin PF, de Krijger RR, Gimenez-Roqueplo AP, Dinjens WN | title = Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas | journal = The Journal of Clinical Endocrinology and Metabolism | volume = 95 | issue = 3 | pages = 1274–8 | date = March 2010 | pmid = 19915015 | doi = 10.1210/jc.2009-2170 | doi-access = free }}
* {{cite journal | vauthors = Milosevic D, Lundquist P, Cradic K, Vidal-Folch N, Huynh T, Pacak K, Grebe SK | title = Development and validation of a comprehensive mutation and deletion detection assay for SDHB, SDHC, and SDHD | journal = Clinical Biochemistry | volume = 43 | issue = 7–8 | pages = 700–4 | date = May 2010 | pmid = 20153743 | pmc = 3419008 | doi = 10.1016/j.clinbiochem.2010.01.016 }}
* {{cite journal | vauthors = Janecke AR, Willett-Brozick JE, Karas C, Hasipek M, Loeffler-Ragg J, Baysal BE | title = Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria | journal = Journal of Human Genetics | volume = 55 | issue = 3 | pages = 182–5 | date = March 2010 | pmid = 20111059 | doi = 10.1038/jhg.2009.142 | doi-access = free }}
* {{cite journal | vauthors = Cascón A, López-Jiménez E, Landa I, Leskelä S, Leandro-García LJ, Maliszewska A, Letón R, de la Vega L, García-Barcina MJ, Sanabria C, Alvarez-Escolá C, Rodríguez-Antona C, Robledo M | title = Rationalization of genetic testing in patients with apparently sporadic pheochromocytoma/paraganglioma | journal = Hormone and Metabolic Research | volume = 41 | issue = 9 | pages = 672–5 | date = September 2009 | pmid = 19343621 | doi = 10.1055/s-0029-1202814 | s2cid = 24979281 }}
* {{cite journal | vauthors = Waldmann J, Langer P, Habbe N, Fendrich V, Ramaswamy A, Rothmund M, Bartsch DK, Slater EP | title = Mutations and polymorphisms in the SDHB, SDHD, VHL, and RET genes in sporadic and familial pheochromocytomas | journal = Endocrine | volume = 35 | issue = 3 | pages = 347–55 | date = June 2009 | pmid = 19399650 | doi = 10.1007/s12020-009-9178-y | s2cid = 8986765 }}
* {{cite journal | vauthors = Ricketts CJ, Forman JR, Rattenberry E, Bradshaw N, Lalloo F, Izatt L, Cole TR, Armstrong R, Kumar VK, Morrison PJ, Atkinson AB, Douglas F, Ball SG, Cook J, Srirangalingam U, Killick P, Kirby G, Aylwin S, Woodward ER, Evans DG, Hodgson SV, Murday V, Chew SL, Connell JM, Blundell TL, Macdonald F, Maher ER | title = Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD | journal = Human Mutation | volume = 31 | issue = 1 | pages = 41–51 | date = January 2010 | pmid = 19802898 | doi = 10.1002/humu.21136 | s2cid = 22888808 | doi-access = free }}
* {{cite journal | vauthors = Gill AJ, Benn DE, Chou A, Clarkson A, Muljono A, Meyer-Rochow GY, Richardson AL, Sidhu SB, Robinson BG, Clifton-Bligh RJ | title = Immunohistochemistry for SDHB triages genetic testing of SDHB, SDHC, and SDHD in paraganglioma-pheochromocytoma syndromes | journal = Human Pathology | volume = 41 | issue = 6 | pages = 805–14 | date = June 2010 | pmid = 20236688 | doi = 10.1016/j.humpath.2009.12.005 }}
* {{cite journal | vauthors = Martin TP, Irving RM, Maher ER | title = The genetics of paragangliomas: a review | journal = Clinical Otolaryngology | volume = 32 | issue = 1 | pages = 7–11 | date = February 2007 | pmid = 17298303 | doi = 10.1111/j.1365-2273.2007.01378.x | doi-access = free }}
* {{cite journal | vauthors = Eng C, Kiuru M, Fernandez MJ, Aaltonen LA | title = A role for mitochondrial enzymes in inherited neoplasia and beyond | journal = Nature Reviews. Cancer | volume = 3 | issue = 3 | pages = 193–202 | date = March 2003 | pmid = 12612654 | doi = 10.1038/nrc1013 | s2cid = 20549458 }}
* {{cite journal | vauthors = Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD | title = Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip | journal = American Journal of Human Genetics | volume = 85 | issue = 5 | pages = 628–42 | date = November 2009 | pmid = 19913121 | pmc = 2775832 | doi = 10.1016/j.ajhg.2009.10.014 }}
* {{cite journal | vauthors = Hermsen MA, Sevilla MA, Llorente JL, Weiss MM, Grimbergen A, Allonca E, Garcia-Inclán C, Balbín M, Suárez C | title = Relevance of germline mutation screening in both familial and sporadic head and neck paraganglioma for early diagnosis and clinical management | journal = Cellular Oncology | volume = 32 | issue = 4 | pages = 275–83 | date = January 2010 | pmid = 20208144 | pmc = 4619289 | doi = 10.3233/CLO-2009-0498 }}
* {{cite journal | vauthors = Hensen EF, Jansen JC, Siemers MD, Oosterwijk JC, Vriends AH, Corssmit EP, Bayley JP, van der Mey AG, Cornelisse CJ, Devilee P | title = The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family | journal = European Journal of Human Genetics | volume = 18 | issue = 1 | pages = 62–6 | date = January 2010 | pmid = 19584903 | pmc = 2987152 | doi = 10.1038/ejhg.2009.112 }}
* {{cite journal | vauthors = Brière JJ, Favier J, El Ghouzzi V, Djouadi F, Bénit P, Gimenez AP, Rustin P | title = Succinate dehydrogenase deficiency in human | journal = Cellular and Molecular Life Sciences | volume = 62 | issue = 19–20 | pages = 2317–24 | date = October 2005 | pmid = 16143825 | doi = 10.1007/s00018-005-5237-6 | s2cid = 23793565 | pmc = 11139140 }}
* {{cite journal | vauthors = Richalet JP, Gimenez-Roqueplo AP, Peyrard S, Vénisse A, Marelle L, Burnichon N, Bouzamondo A, Jeunemaitre X, Azizi M, Elghozi JL | title = A role for succinate dehydrogenase genes in low chemoresponsiveness to hypoxia? | journal = Clinical Autonomic Research | volume = 19 | issue = 6 | pages = 335–42 | date = December 2009 | pmid = 19768395 | doi = 10.1007/s10286-009-0028-z | s2cid = 2265162 }}
* {{cite journal | vauthors = Sevilla MA, Hermsen MA, Weiss MM, Grimbergen A, Balbín M, Llorente JL, Rodrigo JP, Suárez C | title = Chromosomal changes in sporadic and familial head and neck paragangliomas | journal = Otolaryngology–Head and Neck Surgery | volume = 140 | issue = 5 | pages = 724–9 | date = May 2009 | pmid = 19393419 | doi = 10.1016/j.otohns.2009.01.004 | s2cid = 5393912 }}
* {{cite journal | vauthors = Hendrickson SL, Lautenberger JA, Chinn LW, Malasky M, Sezgin E, Kingsley LA, Goedert JJ, Kirk GD, Gomperts ED, Buchbinder SP, Troyer JL, O'Brien SJ | title = Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression | journal = PLOS ONE | volume = 5 | issue = 9 | pages = e12862 | date = September 2010 | pmid = 20877624 | pmc = 2943476 | doi = 10.1371/journal.pone.0012862 | bibcode = 2010PLoSO...512862H | doi-access = free }}
* {{cite journal | vauthors = Erlic Z, Rybicki L, Peczkowska M, Golcher H, Kann PH, Brauckhoff M, Müssig K, Muresan M, Schäffler A, Reisch N, Schott M, Fassnacht M, Opocher G, Klose S, Fottner C, Forrer F, Plöckinger U, Petersenn S, Zabolotny D, Kollukch O, Yaremchuk S, Januszewicz A, Walz MK, Eng C, Neumann HP | title = Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients | journal = Clinical Cancer Research | volume = 15 | issue = 20 | pages = 6378–85 | date = October 2009 | pmid = 19825962 | doi = 10.1158/1078-0432.CCR-09-1237 | s2cid = 6225809 | doi-access =  }}
* {{cite journal | vauthors = Krawczyk A, Hasse-Lazar K, Pawlaczek A, Szpak-Ulczok S, Krajewska J, Paliczka-Cieślak E, Jurecka-Lubieniecka B, Roskosz J, Chmielik E, Ziaja J, Cierpka L, Peczkowska M, Preibisz A, Januszewicz A, Otto M, Jarzab B | title = Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas | journal = Endokrynologia Polska | volume = 61 | issue = 1 | pages = 43–8 | year = 2010 | pmid = 20205103 }}
* {{cite journal | vauthors = Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S | title = Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study | journal = Diabetes Care | volume = 33 | issue = 10 | pages = 2250–3 | date = October 2010 | pmid = 20628086 | pmc = 2945168 | doi = 10.2337/dc10-0452 }}
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