Talk:C9orf72
Latest comment: 11 years ago by Greensborough in topic Clinical significance
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Clinical significance
edit"The mutations in C9ORF72 are significant because it is the first pathogenic mechanism identified to be a genetic link between familial frontotemporal dementia and amyotrophic lateral sclerosis" I believe this may need reviewing, as mutations in TARDBP and FUS also provide a genetic link between familial frontotemporal dementia and amyotrophic lateral sclerosis. (Rethinking ALS: The FUS about TDP-43) Greensborough (talk) 13:40, 23 March 2013 (UTC)