Open AccessA severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia
Author(s) -
AmritBhangoo AmritBhangoo,
PeterZhan TaoWang,
IreneYoung IreneYoung,
AaronSassoon AaronSassoon,
RobertoTaguibao RobertoTaguibao,
AntoineKhoury AntoineKhoury
Publication year - 2018
Publication title -
international journal of medical reviews and case reports
Language(s) - English
Resource type - Journals
ISSN - 2534-9821
DOI - 10.5455/ijmrcr.leydig-cell-hyperplasia-mutation
Subject(s) - leydig cell , mutation , hyperplasia , gene , gene mutation , medicine , endocrinology , biology , genetics , hormone , luteinizing hormone