Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay. | Br J Dermatol;165(5): 1127-32, 2011 Nov. | MEDLINE

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Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay.

Refke, M; Pasternack, S M; Fiebig, B; Wenzel, S; Ishorst, N; Ludwig, M; Nöthen, M M; Seyger, M M; Hamel, B C; Betz, R C.

Affiliation

Refke M; Institute of Human Genetics, University of Bonn, Bonn, Germany.

Br J Dermatol ; 165(5): 1127-32, 2011 Nov.

Article in En | MEDLINE | ID: mdl-21718278

Subject(s)

Alopecia/genetics; Mutation/genetics; Transcription Factors/genetics; Alopecia/congenital; Child; DNA, Complementary/genetics; Exons/genetics; Female; Humans; Infant; RNA Splice Sites

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Full text: 1 Database: MEDLINE Main subject: Transcription Factors / Alopecia / Mutation Type of study: Prognostic_studies Limits: Child / Female / Humans / Infant Language: En Year: 2011 Type: Article

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Full text: 1 Database: MEDLINE Main subject: Transcription Factors / Alopecia / Mutation Type of study: Prognostic_studies Limits: Child / Female / Humans / Infant Language: En Year: 2011 Type: Article