Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders

Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders

Introduction: Inherited myotonic disorders are genetically heterogeneous and associated with overlapping clinical features of muscle stiffness, weakness, and pain. Data on genotype-phenotype correlations are limited. In this study, clinical features and treatment patterns in genetically characterize...

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Bibliographic Details
Main Authors: Alayne P. Meyer, Jennifer Roggenbuck, Samantha LoRusso, John Kissel, Rachel M. Smith, David Kline, W. David Arnold
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-06-01
Series:Frontiers in Neurology
Subjects:
myotonia
channelopathies
inherited
treatment
genotype-phenotype
myotonic dystrophy
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2020.00593/full

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https://www.frontiersin.org/article/10.3389/fneur.2020.00593/full

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