Keratin 16 and keratin 17 mutations cause pachyonychia congenita.

McLean, W H; Rugg, E L; Lunny, D P; Morley, S M; Lane, E B; Swensson, O; Dopping-Hepenstal, P J; Griffiths, W A; Eady, R A; Higgins, C

McLean, W H; Rugg, E L; Lunny, D P; Morley, S M; Lane, E B; Swensson, O; Dopping-Hepenstal, P J; Griffiths, W A; Eady, R A; Higgins, C.

Affiliation

McLean WH; Dept of Anatomy Physiology, University of Dundee, UK.

Nat Genet ; 9(3): 273-8, 1995 Mar.

Article in En | MEDLINE | ID: mdl-7539673

Subject(s)

Ectodermal Dysplasia/genetics; Keratins/genetics; Mutation; Amino Acid Sequence; Base Sequence; DNA/genetics; DNA Primers/genetics; Ectodermal Dysplasia/classification; Ectodermal Dysplasia/pathology; Female; Genes, Dominant; Genotype; Heterozygote; Humans; Male; Molecular Sequence Data; Pedigree; Phenotype; Polymerase Chain Reaction

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Collection: 01-internacional Database: MEDLINE Main subject: Ectodermal Dysplasia / Keratins / Mutation Limits: Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1995 Document type: Article Affiliation country: United kingdom Country of publication: United States

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