1. Whole exome sequencing identifies a novel compound heterozygous GFM1 variant underlying developmental delay, dystonia, polymicrogyria, and severe intellectual disability in a Pakhtun family. Issue 9 (15th June 2022) Authors: Khan, Atta Ullah; Khan, Ibrar; Khan, Muhammad Ismail; Latif, Muhammad; Siddiqui, Muhammad Imran; Khan, Shafi Ullah; Htar, Thet Thet; Wahid, Ghazala; Ullah, Ikram; Bibi, Fehmida; Khan, Asifullah; Naseer, Muhammad Imran; Seo, Go Hun; Jelani, Musharraf Journal: American journal of medical genetics Issue: Volume 188:Issue 9(2022) Page Start: 2693 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗