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[P3–112]: INVESTIGATING GENETIC VARIATION IN ALZHEIMER's DISEASE USING WHOLE‐EXOME SEQUENCING
Author(s) -
Patel Tulsi,
Brookes Keeley J.,
GuettaBaranes Tamar,
Chappell Sally,
Guerreiro Rita,
Bras Jose T.,
Hardy John,
Francis Paul T.,
Morgan Kevin
Publication year - 2017
Publication title -
alzheimer's and dementia
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2017.06.1323
Subject(s) - psen1 , exome sequencing , exome , biology , missense mutation , genome wide association study , genetics , frontotemporal dementia , frameshift mutation , genetic association , dementia , disease , trem2 , alzheimer's disease , gene , computational biology , bioinformatics , phenotype , medicine , single nucleotide polymorphism , genotype , amyloid precursor protein , receptor , myeloid cells
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