Correction of pseudoexon splicing caused by a novel intronic dysferlin mutation

Author:

Dominov Janice A.1,Uyan Özgün1,McKenna‐Yasek Diane1,Nallamilli Babi Ramesh Reddy2,Kergourlay Virginie3,Bartoli Marc3,Levy Nicolas34,Hudson Judith5,Evangelista Teresinha6,Lochmuller Hanns678910,Krahn Martin34,Rufibach Laura11,Hegde Madhuri2,Brown Robert H.1

Affiliation:

1. Department of Neurology University of Massachusetts Medical School Worcester Massachusetts

2. Department of Human Genetics Emory University School of Medicine Atlanta Georgia

3. Marseille Medical Genetics ‐ Translational Neuromyology Aix‐Marseille Univ INSERM MMG Marseille France

4. Département de Génétique Médicale APHM Hôpital Timone Enfants Marseille France

5. Northern Molecular Genetics Service Newcastle upon Tyne United Kingdom

6. Newcastle University John Walton Centre for Muscular Dystrophy Research MRC Centre for Neuromuscular Diseases Institute of Genetic Medicine Newcastle upon Tyne United Kingdom

7. Department of Neuropediatrics and Muscle Disorders Faculty of Medicine Medical Center–University of Freiburg Freiburg Germany

8. Centro Nacional de Análisis Genómico (CNAG‐CRG) Center for Genomic Regulation Barcelona Institute of Science and Technology (BIST) Barcelona Catalonia Spain

9. Children's Hospital of Eastern Ontario Research Institute University of Ottawa Ottawa Canada

10. Division of Neurology Department of Medicine The Ottawa Hospital Ottawa Canada

11. Jain Foundation, Inc. Seattle Washington

Funder

National Institute of Neurological Disorders and Stroke

Jain Foundation

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

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