Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s) Article

Weiler, T, Bashir, R, Anderson, LVB et al. (1999). Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s) . HUMAN MOLECULAR GENETICS, 8(5), 871-877. 10.1093/hmg/8.5.871

International Collaboration

cited authors

  • Weiler, T; Bashir, R; Anderson, LVB; Davison, K; Moss, JA; Britton, S; Nylen, E; Keers, S; Vafiadaki, E; Greenberg, CR; Bushby, KMD; Wrogemann, K

sustainable development goals

authors

publication date

  • May 1, 1999

webpage

published in

keywords

  • Biochemistry & Molecular Biology
  • Genetics & Heredity
  • LOCUS
  • Life Sciences & Biomedicine
  • MAPS
  • SKELETAL-MUSCLE
  • Science & Technology

Digital Object Identifier (DOI)

publisher

  • OXFORD UNIV PRESS

start page

  • 871

end page

  • 877

volume

  • 8

issue

  • 5