Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma.

Hunt, D M; Rickman, L; Whittock, N V; Eady, R A; Simrak, D; Dopping-Hepenstal, P J; Stevens, H P; Armstrong, D K; Hennies, H C; Küster, W; Hughes, A E; Arnemann, J; Leigh, I M; McGrath, J A; Kelsell, D P; Buxton, R S

Hunt, D M; Rickman, L; Whittock, N V; Eady, R A; Simrak, D; Dopping-Hepenstal, P J; Stevens, H P; Armstrong, D K; Hennies, H C; Küster, W; Hughes, A E; Arnemann, J; Leigh, I M; McGrath, J A; Kelsell, D P; Buxton, R S.

Affiliation

Hunt DM; Division of Membrane Biology, National Institute for Medical Research, Mill Hill, London, NW7 1AA, UK.

Eur J Hum Genet ; 9(3): 197-203, 2001 Mar.

Article in En | MEDLINE | ID: mdl-11313759

Subject(s)

Cadherins/genetics; Keratoderma, Palmoplantar/genetics; Mutation; Base Sequence; DNA Primers; Desmoglein 1; Exons; Humans; Introns

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Database: MEDLINE Main subject: Cadherins / Keratoderma, Palmoplantar / Mutation Limits: Humans Language: En Year: 2001 Type: Article

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PubMed Links

Database: MEDLINE Main subject: Cadherins / Keratoderma, Palmoplantar / Mutation Limits: Humans Language: En Year: 2001 Type: Article