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A Common Founder Mutation in the EDA-A1 Gene in X-Linked Hypodontia
BACKGROUND: X-linked recessive hypohidrotic ectodermal dysplasia (XLHED; OMIM 305100) is a rare genodermatosis characterized clinically by developmental abnormalities affecting the teeth, hair and sweat glands. Mutations in the EDA-A1 gene have been associated with XLHED. Recently, mutations in the...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
S. Karger AG
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2992807/ https://ncbi.nlm.nih.gov/pubmed/20628232 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000314329 |
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