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Article

[Congenital TSH * PRL combined deficiency (TRH receptor gene mutation)].

Nihon rinsho. Japanese journal of clinical medicine - 28 May 2006

Hashimoto Koshi, Yamada Masanobu

Abstract excerpt

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Topics

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Share to Diagnosis, Differential
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16776099

Genes

PRL
TRH

Provenance

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.

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

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