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Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.
Baysal BE, Ferrell RE, Willett-Brozick JE, Lawrence EC, Myssiorek D, Bosch A, van der Mey A, Taschner PE, Rubinstein WS, Myers EN, Richard CW 3rd, Cornelisse CJ, Devilee P, Devlin B. Baysal BE, et al. Science. 2000 Feb 4;287(5454):848-51. doi: 10.1126/science.287.5454.848. Science. 2000. PMID: 10657297
Germ-line mutations in nonsyndromic pheochromocytoma.
Neumann HP, Bausch B, McWhinney SR, Bender BU, Gimm O, Franke G, Schipper J, Klisch J, Altehoefer C, Zerres K, Januszewicz A, Eng C, Smith WM, Munk R, Manz T, Glaesker S, Apel TW, Treier M, Reineke M, Walz MK, Hoang-Vu C, Brauckhoff M, Klein-Franke A, Klose P, Schmidt H, Maier-Woelfle M, Peçzkowska M, Szmigielski C, Eng C; Freiburg-Warsaw-Columbus Pheochromocytoma Study Group. Neumann HP, et al. N Engl J Med. 2002 May 9;346(19):1459-66. doi: 10.1056/NEJMoa020152. N Engl J Med. 2002. PMID: 12000816 Free article.