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Article

Leydig cell hypoplasia due to inactivation of luteinizing hormone receptor by a novel homozygous nonsense truncation mutation in the seventh transmembrane domain

15 Dec 2004

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Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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Identifiers

PMID: 15607529
DOI: 10.1016/j.mce.2004.09.005

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Leydig cell hypoplasia due to inactivation of luteinizing hormone receptor by a novel homozygous nonsense truncation mutation in the seventh transmembrane domainPMID 15607529Read ↗

A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasiaSemantic proximity Read ↗

A new variant in signal peptide of the human luteinizing hormone receptor (LHCGR) affects receptor biogenesis causing leydig cell hypoplasia.Semantic proximity Read ↗

Leydig cell hypoplasia due to inactivating luteinizing hormone/chorionic gonadotropin receptor gene mutation presenting as a 46,XY DSD.Semantic proximity Read ↗

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A novel double mutation in the luteinizing hormone receptor in a kindred with familial Leydig cell hypoplasia and male pseudohermaphroditism.Semantic proximity Read ↗

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Naturally occurring mutations of the luteinizing hormone receptor gene affecting reproduction.Semantic proximity Read ↗

Compound heterozygous mutations of the luteinizing hormone receptor gene in Leydig cell hypoplasia.Semantic proximity Read ↗

Male pseudohermaphroditism due to inactivating luteinizing hormone receptor mutations.Semantic proximity Read ↗

Naturally occurring mutations of the luteinizing-hormone receptor: lessons learned about reproductive physiology and G protein-coupled receptors.Semantic proximity Read ↗

Mutations in a novel, cryptic exon of the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism.Semantic proximity Read ↗

Insights into the coexistence of two mutations in the same LHCGR gene locus causing severe Leydig cell hypoplasia.Semantic proximity Read ↗

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