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dc.contributor.editorHegde and Arunkanth Ankala, Madhuri
dc.date.accessioned2021-04-20T15:33:33Z
dc.date.available2021-04-20T15:33:33Z
dc.date.issued2012
dc.identifierONIX_20210420_9789535106036_1436
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/66078
dc.description.abstractWith more than 30 different types and subtypes known and many more yet to be classified and characterized, muscular dystrophy is a highly heterogeneous group of inherited neuromuscular disorders. This book provides a comprehensive overview of the various types of muscular dystrophies, genes associated with each subtype, disease diagnosis, management as well as available treatment options. Though each different type and subtype of muscular dystrophy is associated with a different causative gene, the majority of them have overlapping clinical presentations, making molecular diagnosis inevitable for both disease diagnosis as well as patient management. This book discusses the currently available diagnostic approaches that have revolutionized clinical research. Pathophysiology of the different muscular dystrophies, multifaceted functions of the involved genes as well as efforts towards diagnosis and effective patient management, are also discussed. Adding value to the book are the included reports on ongoing studies that show a promise for future therapeutic strategies.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MF Pre-clinical medicine: basic sciences::MFN Medical geneticsen_US
dc.subject.otherMedical genetics
dc.titleMuscular Dystrophy
dc.typebook
oapen.identifier.doi10.5772/1242
oapen.relation.isPublishedBy78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6
oapen.relation.isbn9789535106036
oapen.relation.isbn9789535169949
oapen.imprintIntechOpen
oapen.pages556


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