国际皮肤性病学杂志    2010 36 (5): 296-296   ISSN: 2096-5540  CN: 32-1880/R  

线状表皮松解性表皮痣一例
吴秀娟1,普雄明2
1. 新疆维吾尔自治区人民医院皮肤性病科
2. 新疆维吾尔自治区人民医院
收稿日期 2010-02-20  修回日期 2010-05-04  网络版发布日期 2010-09-15
参考文献  

[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 Ⅱ 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 Ⅱ 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.


通讯作者: 吴秀娟