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Volumn 139, Issue , 2017, Pages 168-176

Whole exome sequencing identification of novel candidate genes in patients with proliferative diabetic retinopathy

Author keywords

Aberrant angiogenesis; Candidate genes; Diabetic retinopathy; Whole exome sequencing

Indexed keywords

ADULT; APOB GENE; ARTICLE; CELL CULTURE; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE COURSE; DNA SPLICING; ENDOTHELIUM CELL; ETHNICITY; FAM132A GENE; FEMALE; FRAMESHIFT MUTATION; GENE; GENE EXPRESSION; GENE IDENTIFICATION; GENETIC VARIABILITY; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; MIDDLE AGED; NAT1 GENE; NON INSULIN DEPENDENT DIABETES MELLITUS; NONSENSE MUTATION; NULL ALLELE; PATHOGENESIS; PHENOTYPE; PHF21A GENE; PKHD1L1 GENE; PRIORITY JOURNAL; PROLIFERATIVE DIABETIC RETINOPATHY; RETINA CELL; RNA SPLICE SITE; SLC5A9 GENE; TMEM217 GENE; VALIDATION PROCESS; VEGFB GENE; VPS13B GENE; WHOLE EXOME SEQUENCING; ZNF600 GENE; DIABETIC RETINOPATHY; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; RETINA NEOVASCULARIZATION;

EID: 85019046056     PISSN: 00426989     EISSN: 18785646     Source Type: Journal    
DOI: 10.1016/j.visres.2017.03.007     Document Type: Article
Times cited : (38)

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