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Paper Details

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles.
Cold Spring Harb Mol Case Stud
24
2019
ABCA7, ABI3, ADAM10, AKAP9, APOE 4 alleles, APP, ARSA, Alzheimer's disease, C9orf72, C9orf72 repeat, CSF1R, GBA, GRID2IP, MAPT, MME, NOTCH3, P, PLCD1, PLD3, PSEN1, Participants, SORL1, TM2D3, TNK1, TREM2, TTC3, VPS13C, atypical dementia, dementia, frontotemporal dementia, genetic variants, memory disorders, patient, patients, risk alleles, unspecified dementia
Author NameAffiliation
Brittany N LasseigneHudsonAlpha Institute for Biotechnology
Ethan G GeierUniversity of California San Francisco
James M HoltHudsonAlpha Institute for Biotechnology
Elizabeth A WortheyHudsonAlpha Institute for Biotechnology
Elizabeth A WortheyHudsonAlpha Institute for Biotechnology
David S GeldmacherUniversity of Alabama at Birmingham
Gregory M CooperHudsonAlpha Institute for Biotechnology
Gregory M CooperHudsonAlpha Institute for Biotechnology
Richard M MyersHudsonAlpha Institute for Biotechnology
Richard M MyersHudsonAlpha Institute for Biotechnology
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