期刊
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
卷 155A, 期 5, 页码 1119-1122出版社
WILEY-BLACKWELL
DOI: 10.1002/ajmg.a.33840
关键词
ectodermal dysplasia; missing teeth; hypodontia; odonto-onycho-dermal dysplasia; tricho-odonto-onycho-dermal dysplasia; nail dysplasia
资金
- Thailand Research Fund (TRF)
- European Community [LSHBCT -2005-019067]
- Faculty of Dentistry, Chiang Mai University
WNT10A has been associated with various syndromes with ectodermal dysplasia from severe autosomal recessive SchO? pf-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. (C) 2011 Wiley-Liss, Inc.
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