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P2‐131: WHOLE‐EXOME SEQUENCING OF HISPANIC EARLY‐ONSET ALZHEIMER DISEASE FAMILIES IDENTIFIES RARE VARIANTS IN MULTIPLE ALZHEIMER'S‐RELATED GENES
Author(s) -
PericakVance Margaret,
Reitz Christiane,
Kunkle Brian W.,
Vardarajan Badri N.,
Kohli Martin A.,
Naj Adam C.,
Whitehead Patrice L.,
Perry William,
Martin Eden,
Beecham Gary,
Gilbert John,
Farrer Lindsay A.,
Haines Jonathan,
Schellenberg Gerard D.,
Mayeux Richard
Publication year - 2014
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2014.05.806
Subject(s) - psen1 , genetics , exome sequencing , candidate gene , biology , exome , missense mutation , early onset alzheimer's disease , gene , trem2 , frameshift mutation , alzheimer's disease , mutation , presenilin , disease , medicine , receptor , myeloid cells , pathology