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Published in 2017 at "Human Molecular Genetics"
DOI: 10.1093/hmg/ddx372
Abstract: Abstract A hexanucleotide repeat expansion mutation in the C9orf72 gene represents a prevalent genetic cause of several neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS) and frontotemporal dementia. Non-canonical translation of this repeat gives rise to…
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Keywords:
toxicity elegans;
age;
containing dipeptides;
arginine containing ... See more keywords