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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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Autori principali: Drögemüller, Cord, Distl, Ottmar, Leeb, Tosso
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2003
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Accesso online: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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