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Published in 2017 at "eNeuro"
DOI: 10.1523/eneuro.0249-16.2017
Abstract: Abstract An intronic hexanucleotide repeat expansion (HRE) mutation in the C9ORF72 gene is the most common cause of familial ALS and frontotemporal dementia (FTD) and is found in ∼7% of individuals with apparently sporadic disease.…
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Keywords:
arginine dipeptide;
proline arginine;
repeat;
arginine ... See more keywords