EDAR mutation in autosomal dominant hypohidrotic ectodermal dysplasia in two Swedish families

BACKGROUND: Hypohidrotic ectodermal dysplasia (HED) is a genetic disorder characterized by defective development of teeth, hair, nails and eccrine sweat glands. Both autosomal dominant and autosomal recessive forms of HED have previously been linked to mutations in the ectodysplasin 1 anhidrotic rec...

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Detaylı Bibliyografya
Asıl Yazarlar: Lind, Lisbet K, Stecksén-Blicks, Christina, Lejon, Kristina, Schmitt-Egenolf, Marcus
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2006
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684249/
https://ncbi.nlm.nih.gov/pubmed/17125505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-7-80
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