Germline SDHD mutation in familial phaeochromocytoma
- 1 April 2001
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 357 (9263) , 1181-1182
- https://doi.org/10.1016/s0140-6736(00)04378-6
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary ParagangliomaScience, 2000
- Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.Journal of Medical Genetics, 1995
- A Report of Familial Carotid Body Tumors and Multiple Extra-Adrenal PheochromocytomasJournal of Urology, 1991
- Familial concurrence of carotid body tumor and pheochromocytomaCancer, 1982