Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNA - Winqvist, Satu; Kärppä, Mikko; Moilanen, Jukka S.; Majamaa, Kari (BMC neurology, 2025)
Keywords: Adult; Age; Analysis; Care and treatment; Cognition & reasoning; Cognition disorders; Cognitive ability; Cognitive dysfunction; Cognitive Dysfunction - diagnosis; Cognitive Dysfunction - genetics; Comparative analysis; Diabetes; DNA, Mitochondrial - genetics; Education; Educational evaluation; Executive function; Female; Genetic variation; Hearing loss; Heteroplasmy; Humans; Kaplan-Meier estimate; Male; Medical research; Medicine; Medicine & Public Health; Medicine, Experimental; MELAS syndrome; Memory; Middle Aged; Mitochondrial DNA; Neurochemistry; Neurology; Neuropsychological Tests; Neuropsychology; Neurosurgery; Patients; Phenotype; Phenotypes; Prevention; Risk factors; Visual perception; Finland; MELAS syndrome; Heteroplasmy; Neuropsychological tests; Kaplan-Meier estimate; Cognitive dysfunction