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Article

WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI).

Clinical genetics - 1 Mar 2018

Guazzarotti L, Tadini G, Mancini G E, Sani I, Pisanelli S, Galderisi F, D'Auria E, Secondi R, Bottero A, Zuccotti G V

Abstract excerpt

Ectodermal dysplasias are a group of genetic disorders defined by ectodermal derivative impairment (EDI). To test the impact of the Wnt/beta-catenin pathway in the genetic screening of EDI, we performed a molecular gene study of WNT10A in 60 subjects from a population of 133 young Italian patients referred for the impairment of at least one major ectodermal-derived structure and who had a previous negative...

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Source

Identifiers

PMID: 28976000
DOI: 10.1111/cge.13147

Genes

EDAR
EDARADD

Provenance

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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WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI).PMID 28976000Read ↗

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