Associated Papers
Novel variant in WNT10A caused short anagen hair syndrome in a Chinese pedigree.
Mo R et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2024
Clinical-Genomic Analysis of 1261 Patients with Ehlers-Danlos Syndrome Outlines an Articulo-Autonomic Gene Network (Entome).
Wilson GN et al.
Current Issues in Molecular Biology, 2024
38534782 (PubMed )
Supplement: cimb-46-00166-s001.zip › cimb-2829607-supplementary.xlsx › S3Tab_EDS-917_DNA_variants
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair loss.
Cesarato N et al.
The British Journal of Dermatology, 2023
Prevalence of WNT10A gene mutations in non-syndromic oligodontia.
Ruiz-Heiland G et al.
Clinical Oral Investigations, 2019
Role of WNT10A in failure of tooth development in humans and zebrafish.
Yuan Q et al.
Molecular Genetics & Genomic Medicine, 2017
29178643 (PubMed )
Supplement: MGG3-5-730-s001.docx
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.
Yang J et al.
Molecular Genetics & Genomic Medicine, 2015
25629078 (PubMed )
Supplement: mgg30003-0040-sd1.docx
Variability in dentofacial phenotypes in four families with WNT10A mutations.
Vink CP et al.
European Journal of Human Genetics : Ejhg, 2014
Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.
Plaisancié J et al.
American Journal of Medical Genetics. Part A, 2013
Mutations in WNT10A are present in more than half of isolated hypodontia cases.
van den Boogaard MJ et al.
Journal of Medical Genetics, 2012
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