Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype Article

Weiler, T, Greenberg, CR, Nylen, E et al. (1996). Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype . American Journal of Human Genetics, 59(4), 872-878.

cited authors

  • Weiler, T; Greenberg, CR; Nylen, E; Halliday, W; Morgan, K; Eggertson, D; Wrogemann, K

sustainable development goals

authors

publication date

  • October 1, 1996

published in

keywords

  • BETA-SARCOGLYCAN
  • DISEQUILIBRIUM
  • DISTAL MYOPATHY
  • DOMINANT FORM
  • FRIEDREICH ATAXIA
  • GENETIC-HETEROGENEITY
  • Genetics & Heredity
  • LOCALIZATION
  • LOCUS
  • Life Sciences & Biomedicine
  • MULTILOCUS LINKAGE ANALYSIS
  • MUTATIONS
  • Science & Technology

start page

  • 872

end page

  • 878

volume

  • 59

issue

  • 4