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Article

Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees.

Clinical genetics - 1 Mar 2011

Basit S, Wali A, Aziz A, Muhammad N, Jelani M, Ahmad W

Abstract excerpt

Hypotrichosis is a human hereditary hair loss disorder in which affected individuals show sparse to complete absence of hair on scalp and/or on different body parts. To date, at least eight isolated autosomal recessive and dominant forms of hypotrichosis loci have been mapped on different human c...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20528890
DOI: 10.1111/j.1399-0004.2010.01455.x

Genes

CDH3
DUSP6
KERA
KITLG
PLEKHG7
VEZT

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20528890-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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