Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia
Several ectodermal dysplasia syndromes, including Ectrodactyly-Ectodermal dysplasia-Clefting (EEC) and Ankyloblepharon-Ectodermal Dysplasia-Clefting (AEC) syndromes, are known to result from mutations in the p63 gene. We investigated whether Rapp-Hodgkin syndrome (RHS) is also caused by mutations in...
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| Main Authors: | , , , |
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| 格式: | Article |
| 語言: | English |
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2014
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| 在線閱讀: | http://www.scopus.com/inward/record.url?eid=2-s2.0-0037493688&partnerID=40&md5=c38ead7b1332a48bcd506fae96d9ecfa http://www.ncbi.nlm.nih.gov/pubmed/12766194 http://cmuir.cmu.ac.th/handle/6653943832/1084 |
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