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在12p11.2-q13鉴定出与先天性隐性鱼鳞病有关的新位点
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作者 mizrachi-koren m. Geiger D. +2 位作者 Indelman m E. Sprecher 罗素菊 《世界核心医学期刊文摘(皮肤病学分册)》 2006年第9期9-9,共1页
Congenital recessive ichthyoses represent a vast and markedly heterogeneous group of diseases that have been mapped to at least seven distinct chromosomal loci. In this study, we ascertained two consanguineous familie... Congenital recessive ichthyoses represent a vast and markedly heterogeneous group of diseases that have been mapped to at least seven distinct chromosomal loci. In this study, we ascertained two consanguineous families presenting with congenital ichthyosis. Using homozygosity mapping,we identified a 6.5 cM homozygous region on 12p11.2- q13 shared by all affected individuals. Multipoint logarithmof odds ratio (LOD)- score analysis placed the new locus between markers D12S345 and D12S390 with a maximum LOD score of 4.79 at marker CH12SSR13. This region harbors PPHLN1, encoding periphilin 1, a protein involved in the cornification process. No deleterious mutations were identified within the coding region of this gene, suggesting the existence of another gene associated with epidermal differentiation on 12p11.2- q13. 展开更多
关键词 先天性鱼鳞病 染色体位点 隐性 鉴定 基因定位 血缘关系 表皮分化 编码区
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