Publication:

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C (2001)

Author(s): Bashir R; Straub V; Anderson LVB; Bushby K; Brockington M; Yuva Y; Prandini P; Brown SC; Torelli S; Benson MA; Herrmann R; Burgunder JM; Fallet S; Romero N; Fardeau M; Storey G; Pollitt C; Richard I; Sewry CA; Voit T; Blake DJ; Muntoni F

      • Date: 01-12-2001
      • Journal: Human Molecular Genetics
      • Volume: 10
      • Issue: 25
      • Pages: 2851-2859
      • Publisher: Oxford University Press
      • Publication type: Article
      • Bibliographic status: Published

      Keywords: LAMININ ALPHA-2-CHAIN GENE MEROSIN DEFICIENCY FUKUYAMA-TYPE DYSTROGLYCAN FAMILY

      Staff

      Professor Katherine Bushby
      Act. Res.Chair of Neuromuscular Genetics

      Professor Volker Straub
      Harold Macmillan Professor of Medicine