Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2-chain

• Main Authors: Allamand, V, Sunada, Y, Salih, M.A.M, Straub, V, Ozo, C.O, Al-Turaiki, M.H.S, Akbar, M, Kolo, T, Colognato, H, Zhang, X, Sorokin, L.M, Yurchenco, P.D, Tryggvason, K, Campbell, K.P
• Other Authors: DUKE-NUS MEDICAL SCHOOL
• Format: Article
• Published: Oxford University Press 2020
• Subjects: dystrophin; laminin; alpha chain; article; Becker muscular dystrophy; case report; consanguinity; controlled study; disease severity; female; gene deletion; human; human tissue; immunohistochemistry; male; muscular dystrophy; phenotype; preschool child; priority journal; protein domain; RNA splicing; Iva
• Online Access: https://scholarbank.nus.edu.sg/handle/10635/181143
• Institution: National University of Singapore

10.1093/hmg/6.5.747