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Wagner M, Laval S, Müller J et al. Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy. F1000Posters 2012, 3:534 (poster)

Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy

Matias Wagner, Steven Laval, Juliane Müller, Hacer Durmus, Piraye Serdaroglu-Oflazer, Hanns Lochmüller1
Published 08 Jun 2012
Author Affiliations
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Published 08 Jun 2012

Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy

[version 1; not peer reviewed]

Matias Wagner, Steven Laval, Juliane Müller, Hacer Durmus, Piraye Serdaroglu-Oflazer, Hanns Lochmüller1
Author Affiliations
1 Institute of Human Genetics, Newcastle University, UK
Presented at
UK Neuromuscular Translational Research Conference 2012
Abstract
Competing Interests

No competing interests were disclosed

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