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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Detalles Bibliográficos
Autores principales: Meyer, Alayne P., Roggenbuck, Jennifer, LoRusso, Samantha, Kissel, John, Smith, Rachel M., Kline, David, Arnold, W. David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332828/
https://www.ncbi.nlm.nih.gov/pubmed/32670189
http://dx.doi.org/10.3389/fneur.2020.00593

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332828/
https://www.ncbi.nlm.nih.gov/pubmed/32670189
http://dx.doi.org/10.3389/fneur.2020.00593

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