A severe case of testotoxicosis in an infant due to a c.1732G>C (p.ASP578His) LHCGR gene mutation associated with nodular Leydig cell hyperplasia
AmritBhangoo, AmritBhangoo, TaoWang, PeterZhan, IreneYoung, IreneYoung, AaronSassoon, AaronSassoon, RobertoTaguibao, RobertoTaguibao, AntoineKhoury, AntoineKhoury
Published in International Journal of Medical Reviews and Case Reports (2018)
Published in International Journal of Medical Reviews and Case Reports (2018)
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