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Article

A case of patient affected by hirsutism carrying the P482S CYP21 gene mutation associated with loss of heterozygosity (LOH).

Clinica chimica acta; international journal of clinical chemistry - 1 Aug 2006

Concolino Paola, Carrozza Cinzia, Minucci Angelo, Santonocito Concetta, Ameglio Franco, Zuppi Cecilia, Capoluongo Ettore

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Identifiers

PMID: 16500637
DOI: 10.1016/j.cca.2006.01.013

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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.

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A case of patient affected by hirsutism carrying the P482S CYP21 gene mutation associated with loss of heterozygosity (LOH).PMID 16500637Read ↗

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