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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Détails bibliographiques
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: 2000
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378055/
https://ncbi.nlm.nih.gov/pubmed/10793007
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