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Article

WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.

European journal of human genetics : EJHG - 1 Dec 2009

Nawaz Sadia, Klar Joakim, Wajid Muhammad, Aslam Muhammad, Tariq Muhammad, Schuster Jens, Baig Shahid Mahmood, Dahl Niklas

Abstract excerpt

Wnt signalling is one of a few pathways that are crucial for controlling genetic programs during embryonic development as well as in adult tissues. WNT10A is expressed in the skin and epidermis and it has shown to be critical for the development of ectodermal appendages. A nonsense mutation in WNT10A was recently identified in odonto-onycho-dermal dysplasia (OODD; MIM 257980), a rare syndrome characterised by...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19471313
DOI: 10.1038/ejhg.2009.81
PMCID: PMC2987016

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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