A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.

Hypotrichosis simplex of the scalp (HSS) is an autosomal dominant form of isolated alopecia causing almost complete loss of scalp hair, with onset in childhood. After exclusion of candidate regions previously associated with hair-loss disorders, we performed a genomewide linkage analysis in two Dani...

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Detalhes bibliográficos
Main Authors: Betz, R C, Lee, Y A, Bygum, A, Brandrup, F, Bernal, A I, Toribio, J, Alvarez, J I, Kukuk, G M, Ibsen, H H, Rasmussen, H B, Wienker, T F, Reis, A, Propping, P, Kruse, R, Cichon, S, Nöthen, M M
Formato: Artigo
Idioma:Inglês
Publicado em: 2000
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378055/
https://ncbi.nlm.nih.gov/pubmed/10793007
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