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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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Detalhes bibliográficos
Main Authors: Drögemüller, Cord, Distl, Ottmar, Leeb, Tosso
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2003
Assuntos:
Acesso em linha: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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