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Article

[Mutations in thyrotropin receptors as a cause of thyroid dysfunction].

Ugeskrift for laeger - 1 Jan 1996

Feldt-Rasmussen U F, Rasmussen A K

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Share to Receptors, Thyrotropin
Share to Thyroid Diseases
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 8560629

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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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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[Mutations in thyrotropin receptors as a cause of thyroid dysfunction].PMID 8560629Read ↗

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Mutations of the Human Thyrotropin Receptor Gene Causing Thyroid Hypoplasia and Persistent Congenital HypothyroidismSemantic proximity Read ↗

Activating mutations of the thyrotropin receptor: a short review with emphasis on some pediatric aspects.Semantic proximity Read ↗

[Disorders caused by mutations of the thyrotropin receptor].Semantic proximity Read ↗

[Impaired sensitivity to thyroid hormone].Semantic proximity Read ↗

Brief report: resistance to thyrotropin caused by mutations in the thyrotropin-receptor gene.Semantic proximity Read ↗

[Pathologic manifestations of hormonal receptor mutations].Semantic proximity Read ↗

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