Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy

  1. Lookup NU author(s)
  2. Matias Wagner
  3. Dr Steven Laval
  4. Dr Juliane Mueller
  5. Dr Hacer Durmus
  6. Professor Hanns Lochmuller
Author(s)Wagner M, Laval S, Mueller J, Durmus H, Serdaroglu-Oflazer P, Lochmuller H
Editor(s)
Publication type Conference Proceedings (inc. Abstract)
Conference NameUnited Kingdom Neuromuscular Translational Research Conference
Conference LocationNewcastle upon Tyne, UK
Year of Conference2012
Date22-23 March 2012
Volume22 (s1)
PagesS31-S32
Series TitleNeuromuscular Disorders
0960-8966
ISBN18732364
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PublisherElsevier Ltd
URLhttp://dx.doi.org/10.1016/S0960-8966(12)70096-2
DOI10.1016/S0960-8966(12)70096-2
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