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Vissing, John; Barresi, Rita; Witting, Nanna; Van Ghelue, Marijke; Gammelgaard, Lise; Bindoff, Laurence A.; Straub, Volker; Lochmüller, Hanns; Hudson, Judith; Wahl, Christoph M.; Arnardottir, Snjolaug; Dahlbom, Kathe; Jonsrud, Christoffer; Duno, Morten

A heterozygous 21-bp deletion inCAPN3causes dominantly inherited limb girdle muscular dystrophy

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  • Media type: E-Article
  • Title: A heterozygous 21-bp deletion inCAPN3causes dominantly inherited limb girdle muscular dystrophy
  • Contributor: Vissing, John; Barresi, Rita; Witting, Nanna; Van Ghelue, Marijke; Gammelgaard, Lise; Bindoff, Laurence A.; Straub, Volker; Lochmüller, Hanns; Hudson, Judith; Wahl, Christoph M.; Arnardottir, Snjolaug; Dahlbom, Kathe; Jonsrud, Christoffer; Duno, Morten
  • imprint: Oxford University Press (OUP), 2016
  • Published in: Brain
  • Language: English
  • DOI: 10.1093/brain/aww133
  • ISSN: 0006-8950; 1460-2156
  • Origination:
  • Footnote:
  • Access State: Open Access