1. A homozygous missense variant in the homeobox domain of the NKX6‐2 results in progressive spastic ataxia type 8 associated with lower limb weakness and neurological manifestations. (16th April 2020) Authors: Almatrafi, Ahmad; Umair, Muhammad; Eldardear, Amr; Al‐Luqmani, Majid; Hashmi, Jamil A.; Albalawi, Alia M.; Alfadhel, Majid; Ramzan, Khushnooda; Basit, Sulman Journal: Journal of gene medicine Issue: Volume 22:Number 8(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗