1. A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees. Issue 2 (25th October 2021) Authors: Khan, Kamal; Mehmood, Sarmad; Liu, Chunyu; Siddiqui, Maimoona; Ahmad, Arsalan; Faiz, Belqees Yawar; Chioza, Barry A.; Baple, Emma A.; Ullah, Muhammad I.; Akram, Zaineb; Satti, Humayoon S.; Khan, Raees; Harlalka, Gaurav V.; Jameel, Muhammad; Akram, Talia; Baig, Shahid M.; Crosby, Andrew H.; Hassan... Journal: American journal of medical genetics Issue: Volume 188:Issue 2(2022) Page Start: 498 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗