Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations
We report on three novel (IVS2+1G>A splice site, c.1066G>T, and c.1039G>T, and one previously reported (c.637G>A) WNT10A mutations in three patients affected with odonto-onycho-dermal dysplasia (OODD; OMIM 275980). OODD is a rare form of autosomal recessive ectodermal dysplasia involving...
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| Main Authors: | , , , |
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| 格式: | Article |
| 語言: | English |
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Wiley-Liss Inc.
2014
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| 在線閱讀: | http://www.scopus.com/inward/record.url?eid=2-s2.0-84896315418&partnerID=40&md5=47b7cb203f370f3817d1dee892e8ce3f http://cmuir.cmu.ac.th/handle/6653943832/1187 |
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