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Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy

Lookup NU author(s): Matias Wagner, Dr Steven Laval, Dr Juliane Mueller, Dr Hacer Durmus, Professor Hanns Lochmuller


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Publication metadata

Author(s): Wagner M, Laval S, Mueller J, Durmus H, Serdaroglu-Oflazer P, Lochmuller H

Publication type: Conference Proceedings (inc. Abstract)

Publication status: Published

Conference Name: United Kingdom Neuromuscular Translational Research Conference

Year of Conference: 2012

Pages: S31-S32

ISSN: 0960-8966

Publisher: Elsevier Ltd


DOI: 10.1016/S0960-8966(12)70096-2

Library holdings: Search Newcastle University Library for this item

Series Title: Neuromuscular Disorders

ISBN: 18732364