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An Up-to-Date Overview of the Complexity of Genotype-Phenotype Relationships in Myotonic Channelopathies

Myotonic disorders are inherited neuromuscular diseases divided into dystrophic myotonias and non-dystrophic myotonias (NDM). The latter is a group of dominant or recessive diseases caused by mutations in genes encoding ion channels that participate in the generation and control of the skeletal musc...

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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: Morales, Fernando, Pusch, Michael
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6978732/
https://ncbi.nlm.nih.gov/pubmed/32010054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.01404
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