Genetics of vascular dementia - review from the ICVD working group

• Main Authors: Ikram, M.A, Bersano, A, Manso-Calderón, R, Jia, J.-P, Schmidt, H, Middleton, L, Nacmias, B, Siddiqi, S, Adams, H.H.H
• Other Authors: DUKE-NUS MEDICAL SCHOOL
• Format: Review
• Published: 2020
• Subjects: Alzheimer disease; autosomal dominant disorder; autosomal recessive disorder; CADASIL; CARASIL; cerebrovascular accident; cerebrovascular disease; COL4A1 gene; disease association; Fabry disease; gene; gene identification; genetics; genome-wide association study; GLA gene; HTRA1 gene; human; monogenic disorder; multiinfarct dementia; NOTCH3 gene; phenotype; retinal vasculopathy with cerebral leukodystrophy; Review; TREX1 gene; dementia; diagnostic imaging; disease course; genetic polymorphism; nuclear magnetic resonance imaging; apolipoprotein E; aryldialkylphosphatase; Apolipoproteins E; Aryldialkylphosphatase; Dementia; Dementia, Vascular; Disease Progression; Humans; Magnetic Resonance Imaging; Polymorphism, Genetic
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/179519
• Institution: National University of Singapore

10.1186/s12916-017-0813-9