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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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Bibliografske podrobnosti
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
Format: Artigo
Jezik:Inglês
Izdano: 2000
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378055/
https://ncbi.nlm.nih.gov/pubmed/10793007
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