p(HGNC:APP, var("?")) increases path(MESH:"Alzheimer Disease")

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PubMed:18650430

More than 25 mutations in APP have been identified that are causative of the hereditary form of familial AD and a related condition of hereditary cerebral amyloid angiopathy.

Related Edges 1

• p(HGNC:APP, var("?")) increases path(MESH:"Cerebral Amyloid Angiopathy, Familial")

Confidence

Medium

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