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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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Autores principales: Drögemüller, Cord, Distl, Ottmar, Leeb, Tosso
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2003
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Acceso en línea: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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