[an error occurred while processing this directive] ����Ƥ���Բ�ѧ��־ 2010, 36(5) 296-296 DOI:     ISSN: 2096-5540 CN: 32-1880/R

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PubMed
Article by Wu,X.J
Article by Pu,X.M

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[1] Irvine A.D.,Mclean W.H.I.(1999) Human Keritin disease:the increasing spectrum of disease and subtlety of the phenotype-genotype correlation.Br J Dermatol, 140, 815-828. [2] Fuchs,E.,Esteves,R.A.,Coulombe,P.A.(1992)Transgenic mice expressing a mutant keratin 10 gene reveal the likely genetic basis for epidermolytic hyperkeratosis.Proc Natl Acad Sci USA,89,6906-6910. [3] Compton,J.G.,Digiovanna,J.J.,Santucci,S.K.et al(1992)Linkage of epidermolytic hyperkeratosis to the type �� keratin gene cluster on chromosome 12q.Nat Genet,1,301-305. [4]Bonifas,J.M.,Chen,M.A.et al(1992) Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type �� keratin gene cluster on chromosome 12q.J Invest Dermatol,99,524-527. [5] Paller,A.S.,Syder,A.J.,Chan,Y.M. et al (1994)Genetic and clinical mosaicism in a type of epidermal neves.N Engl J Med,331,1408-1415. [6] Moss,C.,Jones,D.O.,Blight,A.et al(1995)Birthmark due to cutaneous mosaicism for keratin 10 mutation.Lancet,345,596.

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