1. Rare phenotype of ALS4 associated with heterozygous missense mutation c.5842A > G/p.M1948V in helicase domain of SETX gene. Issue 3 (2nd April 2020) Authors: Andreini, I.; Moro, F.; Africa, L.M.; Rubegni, A.; Santorelli, F.M.; Scarpini, C.; Sicurelli, F.; Battisti, C. Journal: Amyotrophic lateral sclerosis and frontotemporal degeneration Issue: Volume 21:Issue 3/4(2020) Page Start: 312 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗