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Association of genetic variants at CETP, AGER, and CYP4F2 locus with the risk of atrophic age-related macular degeneration.
Molecular Genetics & Genomic Medicine ( IF 1.5 ) Pub Date : 2020-07-14 , DOI: 10.1002/mgg3.1357 Rasa Liutkeviciene 1, 2 , Alvita Vilkeviciute 1 , Loresa Kriauciuniene 1, 2 , Mantas Banevicius 2 , Brigita Budiene 2 , Daiva Stanislovaitiene 2 , Reda Zemaitiene 2 , Vytenis P Deltuva 1
Molecular Genetics & Genomic Medicine ( IF 1.5 ) Pub Date : 2020-07-14 , DOI: 10.1002/mgg3.1357 Rasa Liutkeviciene 1, 2 , Alvita Vilkeviciute 1 , Loresa Kriauciuniene 1, 2 , Mantas Banevicius 2 , Brigita Budiene 2 , Daiva Stanislovaitiene 2 , Reda Zemaitiene 2 , Vytenis P Deltuva 1
Affiliation
Age‐related macular degeneration (AMD) is the leading cause of blindness in the elderly individuals. The etiology of AMD includes environmental and genetic factors.
中文翻译:
CETP,AGER和CYP4F2位点的遗传变异与萎缩性年龄相关性黄斑变性的风险相关。
年龄相关性黄斑变性(AMD)是老年人失明的主要原因。AMD的病因包括环境和遗传因素。
更新日期:2020-09-14
中文翻译:
CETP,AGER和CYP4F2位点的遗传变异与萎缩性年龄相关性黄斑变性的风险相关。
年龄相关性黄斑变性(AMD)是老年人失明的主要原因。AMD的病因包括环境和遗传因素。