1. A founder noncoding GALT variant interfering with splicing causes galactosemia. Issue 6 (21st August 2020) Authors: Latchman, Kumarie; Brown, Jeanette; Sineni, Claire J.; Ragin‐Dames, Lorrien; Guo, Shengru; Huang, Jingyu; Thorson, Willa; Hacker, Stephanie; Barbouth, Deborah; Tekin, Mustafa; Bademci, Guney Journal: Journal of inherited metabolic disease Issue: Volume 43:Issue 6(2020) Page Start: 1199 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗