Myelin loss in C9orf72 hexanucleotide expansion carriers
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DOI: 10.1002/jnr.25100
Abstract: The most frequent genetic cause of frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS) is the hexanucleotide repeat expansion in C9orf72. An important neuropathological hallmark associated with this mutation is the accumulation of the… read more here.
Keywords: myelin loss; frcx; loss; c9orf72 ... See more keywords