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Rare Diseases Volume 4, 2016 - Issue 1
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Addendum

Staufen1s role as a splicing factor and a disease modifier in Myotonic Dystrophy Type I

Emma Bondy-ChorneyDepartment of Cellular and Molecular Medicine, University of Ottawa, Center for Neuromuscular Disease, Ottawa, Ontario, Canada
,
Tara E. Crawford ParksDepartment of Cellular and Molecular Medicine, University of Ottawa, Center for Neuromuscular Disease, Ottawa, Ontario, Canada
,
Aymeric Ravel-ChapuisDepartment of Cellular and Molecular Medicine, University of Ottawa, Center for Neuromuscular Disease, Ottawa, Ontario, Canada
,
Bernard J. JasminDepartment of Cellular and Molecular Medicine, University of Ottawa, Center for Neuromuscular Disease, Ottawa, Ontario, Canada
&
Jocelyn CôtéDepartment of Cellular and Molecular Medicine, University of Ottawa, Center for Neuromuscular Disease, Ottawa, Ontario, CanadaCorrespondence[email protected]
Article: e1225644 | Received 18 May 2016, Accepted 11 Aug 2016, Published online: 12 Sep 2016

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