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Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
Why is this work in the frame?
A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.
Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.
Abstract
No abstract. This is not a gap in this database — OpenAlex has none either. 23.3% of the frame is in this state, and the screen finds HALF as much metaresearch here, so the absence is a measured bias rather than a missing field.
The record
- Venue
- Neuron
- Topic
- Amyotrophic Lateral Sclerosis Research
- Field
- Medicine
- Canadian institutions
- University of British Columbia
- Funders
- National Institute of Neurological Disorders and StrokeNational Institute on AgingCanadian Institutes of Health Research
- Keywords
- C9orf72Frontotemporal dementiaTrinucleotide repeat expansionAmyotrophic lateral sclerosisTARDBPGeneticsBiologyPhenotypeDiseaseGeneDementiaMedicinePathologyAllele
- Has abstract in OpenAlex
- no