1. A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis‐2 with impaired intellectual development. Issue 2 (3rd November 2020) Authors: Zaka, Ayesha; Shahzad, Shaheen; Rao, Hadi Zahid; Hashim, Yasmin; Basit, Sulman Journal: American journal of medical genetics Issue: Volume 185:Issue 2(2021) Page Start: 355 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗