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O1‐09‐05: Novel Rare Variants in Known Genes, a Look Into the Familial Alzheimer Sequencing (FASE) Project
Author(s) -
Fernández Maria Victoria,
Budde John,
Saef Ben,
Carrell David,
Howells Bill,
Del-Aguila Jorge L.,
Ma Shengmei,
Norton Joanne,
Chasse Rachel,
Morris John C.,
Goate Alison,
Cruchaga Carlos
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.2016.06.345
Subject(s) - nonsynonymous substitution , genetics , genome wide association study , exome sequencing , biology , minor allele frequency , gene , mendelian inheritance , exome , disease , allele , mutation , single nucleotide polymorphism , allele frequency , genotype , medicine , genome
Maria Victoria Fern andez, John Budde, Ben Saef, David Carrell, Bill Howells, Jorge L. Del-Aguila, Shengmei Ma, Joanne Norton, Rachel Chasse, John C.Morris, Alison Goate, Carlos Cruchaga and the National Institute on Aging – Late-Onset Alzheimer’s Disease/National Cell Repository for Alzheimer’s Disease (NIA-LOAD/NCRAD) Family Study Group, Washington University School of Medicine, Saint Louis, MO, USA; Knight Alzheimer’s Disease Research Center, St. Louis, MO, USA; Washington University School of Medicine, St. Louis, MO, USA; Mount Sinai School of Medicine, New York, NY, USA; 5 WashingtonUniversity in St. Louis, Saint Louis, MO, USA. Contact e-mail: fernandezv@psychiatry. wustl.edu