Abnormal processing of mutant LH receptors is causing the signalling deficiency in two new mutations identified in a patient with complete Leydig cell hypoplasia.

John Martens, S Lumbroso, M Verhoef-Post, A Richter - Unruh, M Szarras-Czapnik, TE Romer, HG Brunner, Axel Themmen, C Sultan

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)2506-2513
Number of pages8
JournalJournal of Clinical Endocrinology and Metabolism
Volume87
Issue number6
DOIs
Publication statusPublished - 2002

Research programs

  • EMC 02-01-82-01-02

Cite this