APP
From SNPedia
| is a | gene |
| is | mentioned by |
| wikipedia | Amyloid_precursor_protein |
| APP | |
| gopubmed | APP |
| 23andMe | APP |
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.