Rare ABCA7 mutations in Alzheimer's disease and cerebral amyloid angiopathy pathology
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Rare mutations in the ATP binding cassette subfamily A member 7 (ABCA7) gene are known risk factors for Alzheimer's disease (AD). Genetic sequencing in 1372 Belgian patients previously revealed rare ABCA7 mutations in 102 carriers, 58 with a premature termina... ...
