Open AccessOR34-6 A Novel Mechanism of SDH-Deficient Tumorigenesis and Implications for Genetic Testing in Patients with Pheochromocytoma-Paraganglioma
Author(s) -
Sunita M. C. De Sousa,
John Toubia,
Jingua Feng,
Paul Wang,
Tristan Hardy,
Milena Babic,
Joel Geoghegan,
Rachel Hall,
G. B. D. Scott,
Lesley Rawlings,
Andreas Schreiber,
Catherine Luxford,
Roderick CliftonBligh,
Nicola Poplawski,
Hamish S. Scott,
David J. Torpy
Publication year - 2019
Publication title -
journal of the endocrine society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.046
H-Index - 20
ISSN - 2472-1972
DOI - 10.1210/js.2019-or34-6
Subject(s) - sdhb , paraganglioma , biology , sanger sequencing , sdha , genetics , germline , pheochromocytoma , germline mutation , sdhd , cancer research , exon , exome , exome sequencing , gene , mutation , medicine , pathology , endocrinology , gene expression