Mutations inWNT10Aare frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

Mutations inWNT10Aare present in more than half of isolated hypodontia cases

(2012) Marie-José van den Boogaard et al.   JOURNAL OF MEDICAL GENETICS

WNT10A and isolated hypodontia

(2011) Piranit Kantaputra et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mutations inEDARADDaccount for a small proportion of hypohidrotic ectodermal dysplasia cases

(2010) N. Chassaing et al.   BRITISH JOURNAL OF DERMATOLOGY

X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings

(2010) F Clauss et al.   CLINICAL GENETICS

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

(2010) Céline Cluzeau et al.   HUMAN MUTATION

WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes

(2009) Axel Bohring et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Ectodermal dysplasias: Clinical and molecular review

(2009) Átila F. Visinoni et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Reciprocal Requirements for EDA/EDAR/NF-κB and Wnt/β-Catenin Signaling Pathways in Hair Follicle Induction

(2009) Yuhang Zhang et al.   DEVELOPMENTAL CELL

WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome

(2009) Sadia Nawaz et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia

(2008) Annemarie H van der Hout et al.   EUROPEAN JOURNAL OF HUMAN GENETICS