P88 Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy

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Bibliographic Details
Published inNeuromuscular disorders : NMD Vol. 22; pp. S31 - S32
Main Authors Wagner, M, Laval, S, Mueller, J, Durmus, H, Serdaroglu-Oflazer, P, Lochmüller, H
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.03.2012
Subjects
Neurology
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ISSN:0960-8966
1873-2364
DOI:10.1016/S0960-8966(12)70096-2