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11/2018, ISBN 9789811305078, 214
This book provides an essential overview combining both clinical and fundamental research advances in myotonic dystrophy. 
Myotonia atrophica-Treatment
eBook
Brain and Nerve, ISSN 1881-6096, 01/2017, Volume 69, Issue 1, pp. 61 - 69
Journal Article
Neurology and Clinical Neuroscience, ISSN 2049-4173, 03/2019, Volume 7, Issue 2, pp. 88 - 90
We report 2 members of a family with gene mutations for both X‐linked dominant Charcot–Marie–Tooth disease and myotonic dystrophy type 1. The father shows... 
Charcot–Marie–Tooth disease | myotonic dystrophy | hereditary motor and sensory neuropathy | CMT | combined disease | Tin | Mutation
Journal Article
Neuron, ISSN 0896-6273, 08/2012, Volume 75, Issue 3, pp. 437 - 450
Journal Article
Clinical Neurophysiology, ISSN 1388-2457, 2010, Volume 121, Issue 7, pp. e21 - e21
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2009 - 15
Journal Article
Nature Structural & Molecular Biology, ISSN 1545-9993, 07/2011, Volume 18, Issue 7, pp. 840 - 845
Journal Article
Clinical Neurology, ISSN 0009-918X, 2012, Volume 52, Issue 11, pp. 1393 - 1396
Journal Article
Nature Medicine, ISSN 1078-8956, 2011, Volume 17, Issue 6, pp. 720 - 725
Myotonic dystrophy is the most common muscular dystrophy in adults and the first recognized example of an RNA-mediated disease. Congenital myotonic dystrophy... 
MEDICINE, RESEARCH & EXPERIMENTAL | CTG REPEAT | CENTRONUCLEAR MYOPATHY | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MYOTUBULAR MYOPATHY | CELL BIOLOGY | SKELETAL-MUSCLE | MESSENGER-RNA | GENE | CHLORIDE CHANNEL | AMPHIPHYSIN-2 BIN1 | MUTATIONS | Cell Line | RNA-Binding Proteins - physiology | Humans | Alternative Splicing - physiology | Exons - genetics | Muscle Weakness - genetics | Protein Isoforms - physiology | Tumor Suppressor Proteins - physiology | Adaptor Proteins, Signal Transducing - physiology | Myotonic Dystrophy - physiopathology | Animals | Tumor Suppressor Proteins - genetics | Adaptor Proteins, Signal Transducing - genetics | Myotonic Dystrophy - genetics | Mice | Nuclear Proteins - physiology | Muscle Weakness - physiopathology | Nuclear Proteins - genetics | Muscle Fibers, Skeletal - physiology | RNA-Binding Proteins - metabolism | Protein Isoforms - genetics | Muscle weakness | Myotonic dystrophy | RNA | Physiological aspects | Genetic aspects | Research | Risk factors | Musculoskeletal diseases | Musculoskeletal system | Biosynthesis | Protein synthesis | Muscular dystrophy | Index Medicus | Alternative Splicing | Exons | Myotonic Dystrophy | RNA-Binding Proteins | Nuclear Proteins | Life Sciences | Adaptor Proteins, Signal Transducing | Muscle Fibers, Skeletal | Protein Isoforms | Muscle Weakness | Tumor Suppressor Proteins | Cancer | Naturvetenskap | Natural Sciences
Journal Article
Brain and Nerve, ISSN 1881-6096, 11/2011, Volume 63, Issue 11, pp. 1161 - 1168
Journal Article
Muscle & Nerve, ISSN 0148-639X, 05/2018, Volume 57, Issue 5, pp. 742 - 748
Journal Article
Rinsho byori. The Japanese journal of clinical pathology, ISSN 0047-1860, 2014, Volume 62, Issue 3, pp. 246 - 254
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, pp. e33218 - e33218
Journal Article