Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family.

Dai, Ru; Wang, Tingting; Wu, Xianjie

Dai, Ru; Wang, Tingting; Wu, Xianjie.

Afiliación

Dai R; Department of Dermatology, Zhejiang University School of Medicine Second Affiliated Hospital, Hangzhou, Zhejiang, China.
Wang T; Department of Dermatology, Zhejiang University School of Medicine Second Affiliated Hospital, Hangzhou, Zhejiang, China.
Wu X; Department of Dermatology, Zhejiang University School of Medicine Second Affiliated Hospital, Hangzhou, Zhejiang, China. Electronic address: wuxianjie@zju.edu.cn.

An Bras Dermatol ; 99(4): 606-609, 2024.

Article en En | MEDLINE | ID: mdl-38594178

Asunto(s)

Pueblo Asiatico; Moniletrix; Linaje; Femenino; Humanos; Masculino; Pueblo Asiatico/genética; China; Pueblos del Este de Asia; Queratinas Específicas del Pelo; Queratinas Tipo II; Moniletrix/genética; Moniletrix/patología; Mutación; Penetrancia

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Linaje / Pueblo Asiatico / Moniletrix País/Región como asunto: Asia Idioma: En Revista: An Bras Dermatol Año: 2024 Tipo del documento: Article

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