Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/49725
Title: WNT10A and isolated hypodontia
Authors: Piranit Kantaputra
Warissara Sripathomsawat
Keywords: Biochemistry, Genetics and Molecular Biology
Medicine
Issue Date: 1-May-2011
Abstract: 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 isolated hypodontia or microdontia. Here we demonstrate that in addition to MSX1, PAX9, AXIN2, and EDA, mutations in WNT10A can cause isolated hypodontia. © 2011 Wiley-Liss, Inc.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955003002&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/49725
ISSN: 15524833
15524825
Appears in Collections:CMUL: Journal Articles

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