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

✍ Scribed by M. Wagner; S. Laval; J. Mueller; H. Durmus; P. Serdaroglu-Oflazer; H. Lochmüller

Book ID: 117670513
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 65 KB
Volume: 22
Category: Article
ISSN: 0960-8966
DOI: 10.1016/s0960-8966(12)70096-2

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