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EDA Gene Mutations Underlie Non-syndromic Oligodontia
Recent studies have detected mutations in the EDA gene, previously identified as causing X-linked hypohidrotic ectodermal dysplasia (XLHED), in two families with X-linked non-syndromic hypodontia. Notably, all affected males in both families exhibited isolated oligodontia, while almost all female ca...
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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publications
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3317984/ https://ncbi.nlm.nih.gov/pubmed/19278982 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034508328627 |
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