Mutation in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin α2 deficiency and abnormal glycosilation of α-Dystroglycan - Brockington, M; Blake, DJ; Prandini, P; Brown, SC; Torelli, S; Benson, MA; Ponting, CP; Estournet, B; Romero, NB; Mercuri, E; Voit, T; Sewry, CA; Guicheney, P; Muntoni, F (Am J Hum Genet, 2001)