Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2

Hypotrichosis simplex (HS) with and without woolly hair (WH) comprises a group of rare, monogenic disorders of hair loss. Patients present with a diffuse loss of scalp and/or body hair, which usually begins in early childhood and progresses into adulthood. Some of the patients also show hair that is...

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Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: Schlaweck, Annika E., Tazi-Ahnini, Rachid, Ü. Basmanav, F. Buket, Mohungoo, Javed, Pasternack-Ziach, Sandra M., Mattheisen, Manuel, Oprisoreanu, Ana-Maria, Humbatova, Aytaj, Wolf, Sabrina, Messenger, Andrew, Betz, Regina C.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2019
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6886801/
https://ncbi.nlm.nih.gov/pubmed/31790498
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0225943
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