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O1‐09‐02: Whole Exome Sequencing of Late Onset Multiplex Families Identifies Rare Coding Variants in Known and Novel Alzheimer’s Disease Genes
Author(s) -
Cukier Holly N.,
Kunkle Brian W.,
Rolati Sophie,
Whitehead Patrice L.,
Vance Jeffery M.,
Cuccaro Michael L.,
Carney Regina M.,
Gilbert John R.,
Martin Eden R.,
Beecham Gary W.,
Haines Jonathan L.,
Pericak-Vance Margaret A.,
Hamilton-Nelson Kara L.
Publication year - 2016
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.2016.06.342
Subject(s) - exome sequencing , genetics , nonsynonymous substitution , biology , gene , pedigree chart , exome , copy number variation , disease , mutation , medicine , genome , pathology