. . . . . . . "[Our results suggest that APP mutations in the A? coding region favour A?38 accumulation in the brain and that the molecular mechanisms of A? deposition in these patients may be different from those active in patients with familial AD associated with other genetic defects and sporadic AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:10:39+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .