1. Case report and novel treatment of an autosomal recessive Leigh syndrome caused by short‐chain enoyl‐CoA hydratase deficiency. Issue 5 (7th March 2019) Authors: Shayota, Brian J.; Soler‐Alfonso, Claudia; Bekheirnia, Mir Reza; Mizerik, Elizabeth; Boyer, Suzy W.; Xiao, Rui; Yang, Yaping; Elsea, Sarah H.; Scaglia, Fernando Journal: American journal of medical genetics Issue: Volume 179:Issue 5(2019) Page Start: 803 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗