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...

Full description

Saved in:
Bibliographic Details
Main Authors: Kantaputra P., Sripathomsawat W.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955003002&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/43061
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-43061
record_format dspace
spelling th-cmuir.6653943832-430612017-09-28T06:47:01Z WNT10A and isolated hypodontia Kantaputra P. Sripathomsawat W. 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. 2017-09-28T06:47:01Z 2017-09-28T06:47:01Z 2011-05-01 Journal 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/6653943832/43061
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
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 Kantaputra P.
Sripathomsawat W.
spellingShingle Kantaputra P.
Sripathomsawat W.
WNT10A and isolated hypodontia
author_facet Kantaputra P.
Sripathomsawat W.
author_sort Kantaputra P.
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 2017
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79955003002&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/43061
_version_ 1681422307322494976