1. Exome sequencing of a Pakistani family with spastic paraplegia identified an 18 bp deletion in the cytochrome B5 domain of FA2H. (1st February 2021) Authors: Abbas, Safdar; Brugger, Beatrice; Zubair, Muhammad; Gul, Sana; Blatterer, Jasmin; Wenninger, Julian; Rehman, Khurram; Tatrai, Benjamin; Khan, Muzammil Ahmad; Windpassinger, Christian Journal: Neurological research Issue: Volume 43:Number 2(2021) Page Start: 133 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗