Genetic variation at 16q24.2 is associated with small vessel stroke

• Main Authors: Traylor, M, Malik, R, Nalls, M.A
• Other Authors: DUKE-NUS MEDICAL SCHOOL
• Format: Article
• Published: John Wiley and Sons Inc. 2020
• Subjects: histone deacetylase 9; macrophage elastase; messenger RNA; spacer DNA; zinc finger protein; arterial tissue; Article; brain hemorrhage; cerebrovascular disease; chromosome 16q; controlled study; DNA methylation; female; fetus; gene expression; gene frequency; gene linkage disequilibrium; genetic association; genetic variability; genetic variation; genome-wide association study; human; major clinical study; male; onset age; priority journal; single nucleotide polymorphism; white matter; adult; aged; cerebrovascular accident; chromosome 16; gene locus; genetics; lacunar stroke; middle aged; very elderly; Adult; Aged; Aged, 80 and over; Cerebral Small Vessel Diseases; Chromosomes, Human, Pair 16; Female; Genetic Loci; Genetic Variation; Genome-Wide Association Study; Humans; Male; Middle Aged; Stroke; Stroke, Lacunar; Zinc Fingers
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/179225
• Institution: National University of Singapore

10.1002/ana.24840