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Article

Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone.

The New England journal of medicine - 16 Jan 1992

Weiss J, Axelrod L, Whitcomb R W, Harris P E, Crowley W F, Jameson J L

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 1727547
DOI: 10.1056/NEJM199201163260306

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Hypogonadism caused by a single amino acid substitution in the beta subunit of luteinizing hormone.PMID 1727547Read ↗

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An update of the pathophysiology of human gonadotrophin subunit and receptor gene mutations and polymorphisms.Semantic proximity Read ↗

Hypogonadism in a Patient with Two Novel Mutations of the Luteinizing Hormone β-Subunit Gene Expressed in a Compound Heterozygous FormSemantic proximity Read ↗

Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone beta-subunit gene.Semantic proximity Read ↗

Hypogonadism in a Patient with a Mutation in the Luteinizing Hormone Beta-Subunit GeneSemantic proximity Read ↗

Molecular genetics, hypogonadism and luteinizing hormone.Semantic proximity Read ↗

Luteinizing hormone beta mutation and hypogonadism in men and women.Semantic proximity Read ↗

Functional characterization of a natural variant of luteinizing hormone.Semantic proximity Read ↗

A vital region for human glycoprotein hormone trafficking revealed by an LHB mutationSemantic proximity Read ↗

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