Article ID Journal Published Year Pages File Type
6265409 Brain Research 2011 5 Pages PDF
Abstract
►Significant difference was found in genotype (P = 0.003) and allele (P = 0.002) frequencies of the SNP rs760678 within NEDD9 between LOAD patients and controls. ►The C-carrying genotype (GC + CC) individuals showed a 2.25-fold increased risk compared with the GG genotype carriers (P = 0.001). ►The C allele of rs760678 was only significantly associated with LOAD in non-APOE ε4 allele carriers (P = 0.024). ►rs760678 polymorphism was still strongly associated with LOAD after adjustment for age, gender, and the APOEε4 carrier status.
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