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Genetics of myotonic dystrophy (including cDM and DM2).- Basic Molecular pathomechanism.- Clinical features in skeletal muscle and their underlying molecular mechanism.- Clinical features in heart and their underlying molecular mechanism.- Clinical features of central nervous system.- Pathological changes in DM brain.- Molecular defect in DM central nervous system.- Respiratory feature in DM.- Glucose intolerance in DM.- Lipid metabolism in DM.- Dysphagia in DM.- DM patient-derived iPS cells.- Therapeutic development in DM.mehr
Kritik
"This book is suitable for neuromuscular medicine subspecialists, healthcare providers involved in the care of myotonic dystrophy patients, and clinical basic science researchers. The book meets the needs of this audience. ... This book stands out as an excellent reference on myotonic dystrophy." (Eduardo De Sousa, Doody's Book Reviews, June 28, 2019)mehr