A loss of function variant in CASP7 protects against Alzheimer's disease in homozygous APOE ε4 allele carriers.
about
The human-specific CASP4 gene product contributes to Alzheimer-related synaptic and behavioural deficits.Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease.Loss-of-function mutation in Mirta22/Emc10 rescues specific schizophrenia-related phenotypes in a mouse model of the 22q11.2 deletion.
P2860
A loss of function variant in CASP7 protects against Alzheimer's disease in homozygous APOE ε4 allele carriers.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
A loss of function variant in ...... ygous APOE ε4 allele carriers.
@ast
A loss of function variant in ...... ygous APOE ε4 allele carriers.
@en
type
label
A loss of function variant in ...... ygous APOE ε4 allele carriers.
@ast
A loss of function variant in ...... ygous APOE ε4 allele carriers.
@en
prefLabel
A loss of function variant in ...... ygous APOE ε4 allele carriers.
@ast
A loss of function variant in ...... ygous APOE ε4 allele carriers.
@en
P2093
P2860
P1433
P1476
A loss of function variant in ...... ygous APOE ε4 allele carriers.
@en
P2093
Amr H Wardeh
David J Carey
Kristin L Ayers
Michael F Murray
Uyenlinh L Mirshahi
P2860
P2888
P356
10.1186/S12864-016-2725-Z
P407
P478
17 Suppl 2
P577
2016-06-23T00:00:00Z
P6179
1012890273