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

Autoria(s): Hunt, D.M.; Rickman, L.; Whittock, N.V.; Eady, R.A.J.; Simrak, D.; Dopping-Hepenstal, P.J.C.; Stevens, H.P.; Armstrong, D.K.B.; Hennies, H.C.; Kuster, W.; Hughes, Anne; Arnemann, J.; Leigh, I.M.; McGrath, J.A.; Kelsell, D.P.; Buxton, R.S.
Data(s)

2001
Formato

application/pdf
Identificador

http://pure.qub.ac.uk/portal/en/publications/spectrum-of-dominant-mutations-in-the-desmosomal-cadherin-desmoglein-1-causing-the-skin-disease-striate-palmoplantar-keratoderma(72364cc1-19d2-4680-bbad-ce007ed38926).html

http://www.scopus.com/inward/record.url?scp=0035086720&partnerID=8YFLogxK
Idioma(s)

eng
Direitos

info:eu-repo/semantics/restrictedAccess
Fonte

Hunt , D M , Rickman , L , Whittock , N V , Eady , R A J , Simrak , D , Dopping-Hepenstal , P J C , Stevens , H P , Armstrong , D K B , Hennies , H C , Kuster , W , Hughes , A , Arnemann , J , Leigh , I M , McGrath , J A , Kelsell , D P & Buxton , R S 2001 , ' Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma ' European Journal of Human Genetics , vol 9 , no. 3 , pp. 197-203 .
Palavras-Chave #/dk/atira/pure/subjectarea/asjc/2700/2716 #Genetics(clinical)
Tipo

article
Acesso ao item digital