We examined specimens from an OPTN-associated ALS individual using the heterozygous E478G missense mutation and another individual using the homozygous Q398X non-sense mutation of were 14
We examined specimens from an OPTN-associated ALS individual using the heterozygous E478G missense mutation and another individual using the homozygous Q398X non-sense mutation of were 14.5% (9/62 cells) and 15.9% (7/44 cells), respectively, and the ones for cleaved caspase 8 were 14.3% (7/49 cells) and 16.7% (7/42 cells), respectively. neurodegenerative disorders. Initial, mutations in ((((and…