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Filaggrin Gene Mutation c.3321delA is Associated with Dry Phenotypes of Atopic Dermatitis in the Chinese Han Population 被引量:1
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作者 Wei-Long Zhong Xia Wu +7 位作者 BO YU Jie Zhang Wei Zhang Ning Xu Jing Zhou Jie-Cheng Zheng Xiao-Fan Chen Xia Dou 《Chinese Medical Journal》 SCIE CAS CSCD 2016年第12期1498-1500,共3页
INTRODUCTION Atopic dermatitis (AD) is a common chronic inflammatory skin disorder that is characterized by dry skin and disturbed skin barrier functions. Mutations in the filaggrin (FLG) gene, the gene coding pro... INTRODUCTION Atopic dermatitis (AD) is a common chronic inflammatory skin disorder that is characterized by dry skin and disturbed skin barrier functions. Mutations in the filaggrin (FLG) gene, the gene coding profilaggrin/filaggrin, have a great impact on the epidermal barrier function and are an important predisposing factor for AD. However, in both Europeans and Asians, 展开更多
关键词 Atopic Dermatitis c.3321 delA Mutation Filaggrin Gene Genotype-phenotype Correlation unlabeled Probe HighResolution Melting Analysis
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