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P3‐121: RARE FRAMESHIFT AND DIGENIC MUTATIONS CONTRIBUTE TO DISEASE ETIOLOGY IN BELGIAN ALZHEIMER AND FRONTOTEMPORAL DEMENTIA PATIENTS
Author(s) -
Perrone Federica,
Cacace Rita,
Van Mossevelde Sara,
Sleegers Kristel,
Zee Julie,
Van Broeckhoven Christine
Publication year - 2018
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.2018.06.1478
Subject(s) - frameshift mutation , frontotemporal dementia , dementia , mutation , genetics , cohort , psen1 , medicine , disease , haplotype , oncology , biology , alzheimer's disease , gene , amyloid precursor protein , genotype