WNT10A and isolated hypodontia

WNT10A has been associated with various syndromes with ectodermal dysplasia from severe autosomal recessive SchÖpf-Schulz-Passarge syndrome to odonto-onycho-dermal dysplasia and autosomal dominant hypodontia. We report WNT10A mutations in an American family of which four members are affected with is...

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Bibliographic Details
Main Authors: Piranit Kantaputra, Warissara Sripathomsawat
Format: Journal
Published: 2018
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Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955003002&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/49725
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Institution: Chiang Mai University

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