Somatic SDHB mutation in an extraadrenal pheochromocytoma [12]

New England Journal of Medicine

Volumn 357, Issue 3, 2007, Pages 306-308

  Van Nederveen, Francien H ^a   Korpershoek, Esther ^a   Lenders, Jacques W M ^b   De Krijger, Ronald R ^a   Dinjens, Winand N M ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

NEUROFIBROMIN;

ADULT; BLADDER; CASE REPORT; CLINICAL FEATURE; FEMALE; HUMAN; IN SITU HYBRIDIZATION; LETTER; MULTIPLE ENDOCRINE NEOPLASIA; MUTATIONAL ANALYSIS; NEUROFIBROMATOSIS; PHEOCHROMOCYTOMA; PRIORITY JOURNAL; TUMOR CELL; VON HIPPEL LINDAU DISEASE;

EID: 34447520170     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMc070010     Document Type: Letter

References (5)

1. Neumann HPH, Bausch B, McWhinney SR, et al. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 2002;346:1459-66.
2. Neumann HP, Pawlu C, Peczkowska M, et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA 2004;292:943-51.
3. Gimenez-Roqueplo AP, Favier J, Rustin P, et al. Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. Cancer Res 2003;63:5615-21.
4. Gimm O, Armanios M, Dziema H, Neumann HP, Eng C. Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res 2000;60:6822-5.
5. Astuti D, Douglas F, Lennard TW, et al. Germline SDHD mutation in familial phaeochromocytoma. Lancet 2001;357:1181-2.