Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy

Wagner M., Laval S., Mueller J., Durmus H. , Serdaroglu-Oflazer P., Lochmueller H.

United Kingdom Neuromuscular Translational Research Conference, Newcastle-Upon-Tyne, United Kingdom, 22 - 23 March 2012, vol.22 identifier

  • Publication Type: Conference Paper / Summary Text
  • Volume: 22
  • City: Newcastle-Upon-Tyne
  • Country: United Kingdom