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1 Ergebnisse
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Genome sequencing for early-onset or atypical dementia: hig..:
Cochran, J Nicholas
;
McKinley, Emily C
;
Cochran, Meagan
...
qt47t438nr. , 2019
Link:
https://escholarship.org/uc/item/47t438nr
RT Journal T1
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt47t438nr&Exemplar=1&LAN=DE A1 Cochran, J Nicholas A1 McKinley, Emily C A1 Cochran, Meagan A1 Amaral, Michelle D A1 Moyers, Bryan A A1 Lasseigne, Brittany N A1 Gray, David E A1 Lawlor, James MJ A1 Prokop, Jeremy W A1 Geier, Ethan G A1 Holt, James M A1 Thompson, Michelle L A1 Newberry, J Scott A1 Yokoyama, Jennifer S A1 Worthey, Elizabeth A A1 Geldmacher, David S A1 Love, Marissa Natelson A1 Cooper, Gregory M A1 Myers, Richard M A1 Roberson, Erik D PB eScholarship, University of California YR 2019 K1 Biological Sciences K1 Biomedical and Clinical Sciences K1 Genetics K1 Alzheimer's Disease K1 Neurosciences K1 Neurodegenerative K1 Acquired Cognitive Impairment K1 Clinical Research K1 Dementia K1 Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) K1 Human Genome K1 Prevention K1 Aging K1 Brain Disorders K1 Aetiology K1 2.1 Biological and endogenous factors K1 Neurological K1 Good Health and Well Being K1 Aged K1 Alleles K1 Alzheimer Disease K1 Apolipoprotein E4 K1 Base Sequence K1 C9orf72 Protein K1 Chromosome Mapping K1 Female K1 Genetic Association Studies K1 Genetic Predisposition to Disease K1 Genetic Variation K1 Genome-Wide Association Study K1 Humans K1 Male K1 Middle Aged K1 Odds Ratio K1 Penetrance K1 Risk Factors K1 Whole Genome Sequencing K1 frontotemporal dementia K1 Pharmacology and pharmaceutical sciences JF qt47t438nr LK http://dx.doi.org/https://escholarship.org/uc/item/47t438nr DO https://escholarship.org/uc/item/47t438nr SF ELIB - SuUB Bremen
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