Evidence against association of the FE65 gene (APBB1) intron 13 polymorphism in Alzheimer's patients

Neuroscience Letters

Volumn 296, Issue 1, 2000, Pages 17-20

  Guénette, Suzanne Y ^a   Bertram, Lars ^a   Crystal, Adam ^a   Bakondi, Benjamin ^a   Hyman, Bradley T ^a   Rebeck, G William ^a   Tanzi, Rudolph E ^a   Blacker, Deborah ^a,b  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

Alzheimer's disease; APBB1; Case control sample; Family based association; FE65; Polymorphism

Indexed keywords

ADULT; AGED; ALZHEIMER DISEASE; ARTICLE; CHROMOSOME 11P; CONTROLLED STUDY; FAMILY STUDY; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENOTYPE; HUMAN; INTRON; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

AGED; ALLELES; ALZHEIMER DISEASE; CASE-CONTROL STUDIES; GENE FREQUENCY; GENOTYPE; HUMANS; INTRONS; LINKAGE DISEQUILIBRIUM; NERVE TISSUE PROTEINS; NUCLEAR FAMILY; NUCLEAR PROTEINS; POLYMORPHISM, GENETIC; REFERENCE VALUES;

EID: 0034672331     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0304-3940(00)01607-4     Document Type: Article

References (20)

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