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Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
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Novel N-terminal truncating CLCN1 mutation in severe Becker disease
Franziska Hoche1, Kay Seidel, Eduardo Barbosa-Sicard
1Department of Neuropediatrics, Goethe University, Frankfurt am Main, Germany.
Muscle & Nerve
|June 13, 2014
Abstract
No abstract available in PubMed .

