Researchers reveal how a common mutation causes neurodegenerative disease
WORCESTER, MA -- Researchers have determined how the most common gene mutation in amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) disrupts normal cell function, providing insight likely to advance efforts to develop targeted therapies for these brain diseases. Scientists from the University of Massachusetts Medical School (UMMS) and St. Jude Children's Research Hospital led the research, which appeared in the science journal Nature.
Investigators reported evidence that mutation of C9ORF72 interferes with the movement of RNAs and proteins into and ...



