Talk:C9orf72

Clinical significance
"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)