A recurrent rare intronic variant in <scp><i>CAPN3</i></scp> alters <scp>mRNA</scp> splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees
Kamal Khan(Duke University), Tahir Naeem Khan(National University of Medical Sciences), Erica E. Davis(Northwestern University), Humayoon Shafique Satti(National University of Medical Sciences), Muhammad Ikram Ullah(Jouf University), Raees Khan(National University of Medical Sciences), Emma A. Baple(University of Exeter), Zaineb Akram, Muhammad Jawad Hassan(International Islamic University Malaysia), Belqees Yawar Faiz(Shifa Tameer-e-Millat University), Gaurav V. Harlalka(University of Exeter), Andrew H. Crosby(University of Exeter), Sarmad Mehmood(National University of Sciences and Technology), Shahid Mahmood Baig(National Institute for Biotechnology and Genetic Engineering), Barry A. Chioza(University of Exeter), Chunyu Liu(Jiamusi University), Feng Zhang(Affiliated Hospital of North Sichuan Medical College), Talia Akram(Uppsala University), Arsalan Ahmad(Shifa Tameer-e-Millat University), Muhammad Jameel(University of Macau)
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