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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Main Authors: Piranit Kantaputra, Warissara Sripathomsawat
Format: Journal
Published: 2018
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-497252018-09-04T04:26:59Z WNT10A and isolated hypodontia Piranit Kantaputra Warissara Sripathomsawat Biochemistry, Genetics and Molecular Biology Medicine 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. 2018-09-04T04:06:10Z 2018-09-04T04:06:10Z 2011-05-01 Journal 15524833 15524825 2-s2.0-79955003002 10.1002/ajmg.a.33840 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955003002&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/49725
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle Biochemistry, Genetics and Molecular Biology
Medicine
Piranit Kantaputra
Warissara Sripathomsawat
WNT10A and isolated hypodontia
description 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.
format Journal
author Piranit Kantaputra
Warissara Sripathomsawat
author_facet Piranit Kantaputra
Warissara Sripathomsawat
author_sort Piranit Kantaputra
title WNT10A and isolated hypodontia
title_short WNT10A and isolated hypodontia
title_full WNT10A and isolated hypodontia
title_fullStr WNT10A and isolated hypodontia
title_full_unstemmed WNT10A and isolated hypodontia
title_sort wnt10a and isolated hypodontia
publishDate 2018
url 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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