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X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle
Ectodermal dysplasias are a large group of rare genetic disorders characterized by impaired development of hair, teeth, and eccrine glands in humans, mice, and cattle. Here, we review the cloning, mutation analyses, and functional studies of the known causative genes for the X-chromosomal anhidrotic...
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
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BioMed Central
2003
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3231755/ https://ncbi.nlm.nih.gov/pubmed/12927086 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1297-9686-35-S1-S137 |
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