Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease - Schmidt, Helena; Zeginigg, Marion; Wiltgen, Marco; Freudenberger, Paul; Petrovic, Katja; Cavalieri, Margherita; Gider, Pierre; Enzinger, Christian; Fornage, Myriam; Debette, Stephanie; Rotter, Jerome I.; Ikram, Mohammad A.; et al. (Brain (London, England : 1878), 2011)
Keywords: Aged; Aged, 80 and over; Alleles; Biological and medical sciences; Brain - metabolism; Brain - pathology; Cerebral Small Vessel Diseases - genetics; Cerebral Small Vessel Diseases - metabolism; Cerebral Small Vessel Diseases - pathology; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; Exons; Female; Follow-Up Studies; Genetic Association Studies; Genotype; Humans; Hypertension - genetics; Hypertension - metabolism; Hypertension - pathology; Magnetic Resonance Imaging; Male; Medical sciences; Middle Aged; Neurology; Original; Phenotype; Promoter Regions, Genetic; Prospective Studies; Receptor, Notch3; Receptors, Notch - genetics; Receptors, Notch - metabolism; cerebral small vessel disease; ageing; genetics; MRI; Human; NOTCH3; Nervous system diseases; Genetic variant; Ageing; Central nervous system; Nuclear magnetic resonance imaging; Elderly; Encephalon