APP

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wikipediaAmyloid_precursor_protein
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 GeneRIF     351
 dbSNP        351
 PubMed     351
 SADR     351
 HugeNav     351
 HEFalMp     APP


10.1126/science.1168979 ?-Amyloid precursor protein (APP) mutations cause familial Alzheimer's disease with nearly complete penetrance. We found an APP mutation alanine-673->valine-673 (A673V) that causes disease only in the homozygous state, whereas heterozygous carriers were unaffected, consistent with a recessive Mendelian trait of inheritance.