A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions.

Aita, V M; Ahmad, W; Panteleyev, A A; Kozlowska, U; Kozlowska, A; Gilliam, T C; Jablonska, S; Christiano, A M

Aita, V M; Ahmad, W; Panteleyev, A A; Kozlowska, U; Kozlowska, A; Gilliam, T C; Jablonska, S; Christiano, A M.

Affiliation

Aita VM; Department of Genetics and Development, Columbia University, New York, NY 10032, USA.

Exp Dermatol ; 9(2): 157-62, 2000 Apr.

Article in En | MEDLINE | ID: mdl-10772391

Subject(s)

Alopecia/genetics; Cysts/genetics; Mutation, Missense/genetics; Proteins/genetics; Skin Diseases/genetics; Zinc Fingers/genetics; Alopecia/complications; Alopecia/congenital; Alopecia/pathology; Amino Acid Sequence/genetics; Base Sequence/genetics; Child; Cysts/complications; Cysts/pathology; DNA Mutational Analysis; Female; Humans; Molecular Sequence Data; Pedigree; Skin Diseases/complications; Skin Diseases/pathology; Transcription Factors/genetics

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Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases / Proteins / Zinc Fingers / Mutation, Missense / Cysts / Alopecia Type of study: Prognostic_studies / Risk_factors_studies Limits: Child / Female / Humans Language: En Journal: Exp Dermatol Year: 2000 Document type: Article

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