Differential response of C9orf72 transcripts following neuronal depolarization

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 manner. Neuronal activity is a crucial modifier of...

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Bibliographic Details
Main Authors: Layla T. Ghaffari, Davide Trotti, Aaron R. Haeusler
Format: Article
Language:English
Published: Elsevier 2023-06-01
Series:iScience
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004223010362