Curated Information
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Curated Information Page
PubMed Id: 1302033 
Mullan M, et al. (1992) A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. Nat Genet 1, 345-7 1302033
This page summarizes selected information from the record referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2012,40:D261-70). To learn more about the scope of PhosphoSitePlus®, click here.
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K670-sm - APP (human)
Orthologous residues
APP (human): K670‑sm, APP iso4 (human): K595‑sm, APP iso8 (human): K651‑sm, APP iso10 (human): K539‑sm, APP (mouse): K670‑sm, APP iso2 (mouse): K595‑sm, APP (rat): K670‑sm, APP iso2 (rat): K595‑sm
 Methods used to characterize site in vivo mutation of modification site
Associated Diseases
Diseases: Alterations: Comments:
Alzheimer's disease mutation of site

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