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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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Detalhes bibliográficos
Main Authors: Lind, Lisbet K, Stecksén-Blicks, Christina, Lejon, Kristina, Schmitt-Egenolf, Marcus
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2006
Assuntos:
Acesso em linha: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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