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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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Hlavní autoři: Drögemüller, Cord, Distl, Ottmar, Leeb, Tosso
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2003
Témata:
On-line přístup: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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