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pro vyhledávání: '"Davide Trotti"'
Publikováno v:
iScience, Vol 26, Iss 6, Pp 106959- (2023)
Summary: The (G4C2)n nucleotide repeat expansion (NRE) mutation in C9orf72 is the most common genetic cause of ALS and FTD. The biological functions of C9orf72 are becoming understood, but it is unclear if this gene is regulated in a neural-specific
Externí odkaz:
https://doaj.org/article/78e90fa33626418c94ba0b12df73e0b4