Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies.
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| Title: | Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies. |
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| Authors: | Bachinski LL; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Baggerly KA; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Neubauer VL; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Nixon TJ; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Raheem O; Department of Neurology, Tampere University Hospital and Medical School, Tampere, Finland., Sirito M; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Unruh AK; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Zhang J; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Nagarajan L; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA., Timchenko LT; Department of Molecular Physiology & Biophysics, Baylor College of Medicine, Houston, TX, USA., Bassez G; Neuromuscular Reference Center, Henri Mondor University Hospital, INSERM U955, East-Paris University, Créteil, France., Eymard B; Reference Center for Neuromuscular Diseases, Institute of Myology, Pitié-Salpêtrière Hospital, Paris, France., Gamez J; Neuromuscular Disorders Clinic, Neurology Department, Hospital General Vall d'Hebron, Barcelona, Spain., Ashizawa T; Department of Neurology, McKnight Brain Institute, University of Florida, Gainesville, FL, USA., Mendell JR; Division of Child Neurology, Nationwide Childrens Hospital, Ohio State University College of Medicine, Columbus, OH, USA., Udd B; Department of Bioinformatics and Computational Biology, University of Texas MD Anderson Cancer Center, Houston, TX, USA; Folkhälsan Institute of Genetics and Department of Medical Genetics, University of Helsinki, Finland; Department of Neurology, Vasa Central Hospital, Finland., Krahe R; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX, USA; Graduate Programs in Human & Molecular Genetics, University of Texas at Houston Graduate School in Biomedical Sciences, Houston, TX, USA; Graduate Programs in Genes & Development, University of Texas at Houston Graduate School in Biomedical Sciences, Houston, TX, USA. Electronic address: rkrahe@mdanderson.org. |
| Source: | Neuromuscular disorders : NMD [Neuromuscul Disord] 2014 Mar; Vol. 24 (3), pp. 227-40. Date of Electronic Publication: 2013 Nov 15. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Pergamon Press Country of Publication: England NLM ID: 9111470 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-2364 (Electronic) Linking ISSN: 09608966 NLM ISO Abbreviation: Neuromuscul Disord Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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