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Results 1 - 2 of 2 for APP
  1. ... scientific literature. Variants (also called mutations) in the APP gene are the most common cause of hereditary cerebral amyloid angiopathy. APP gene variants cause the Dutch, Italian, Arctic, Iowa, ...
  2. ... the disorder can result from variants in the APP, PSEN1, or PSEN2 genes. When any of these ... of many genes in each cell, including the APP gene, instead of the usual two copies. Although ...