Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer Disease

Neurobiology of Aging

Volumn 33, Issue 2, 2012, Pages

  Cai, Guiqing ^a   Atzmon, Gil ^b   Naj, Adam C ^c   Beecham, Gary W ^c   Barzilai, Nir ^b   Haines, Jonathan L ^d   Sano, Mary ^a,e   Pericak Vance, Margaret ^c   Buxbaum, Joseph D ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^c UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^d VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^e VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

Association; Genetics; Mutation; Rare variation

Indexed keywords

ADAM10 ENDOPEPTIDASE; AMYLOID PRECURSOR PROTEIN; TUMOR NECROSIS FACTOR ALPHA CONVERTING ENZYME;

ADAM10 GENE; ADULT; AGED; ALZHEIMER DISEASE; ARTICLE; CONTROLLED STUDY; EXON; FAMILIAL DISEASE; FEMALE; GENE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; PROTEIN DEGRADATION; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 82755192136     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2010.03.003     Document Type: Article

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