Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix. | Chin Med J (Engl);126(16): 3103-6, 2013 Aug. | MEDLINE

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Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix.

Ye, Zhen-zhen; Nan, Xu; Zhao, Hong-shan; Chen, Xue-rong; Song, Qing-hua.

Affiliation

Ye ZZ; Department of Dermatology, Peking University Third Hospital, Beijing, China.

Chin Med J (Engl) ; 126(16): 3103-6, 2013 Aug.

Article in En | MEDLINE | ID: mdl-23981620

Subject(s)

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Collection: 01-internacional Database: MEDLINE Main subject: Keratins, Hair-Specific / Keratins, Type II / Monilethrix / Mutation Type of study: Diagnostic_studies / Etiology_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Chin Med J (Engl) Year: 2013 Document type: Article Affiliation country:

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Collection: 01-internacional Database: MEDLINE Main subject: Keratins, Hair-Specific / Keratins, Type II / Monilethrix / Mutation Type of study: Diagnostic_studies / Etiology_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: Chin Med J (Engl) Year: 2013 Document type: Article Affiliation country: