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Frontiers in Neurology
(Mar 2020)
Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
Nathaniel Elia,
Nathaniel Elia,
Trystan Nault,
Hugh J. McMillan,
Gail E. Graham,
Lijia Huang,
Stephen C. Cannon
Affiliations
Nathaniel Elia
Department of Physiology, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States
Nathaniel Elia
Molecular, Cellular, and Integrative Physiology Program, UCLA, Los Angeles, CA, United States
Trystan Nault
Division of Neurology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada
Hugh J. McMillan
Division of Neurology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada
Gail E. Graham
Department of Genetics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada
Lijia Huang
Department of Genetics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada
Stephen C. Cannon
Department of Physiology, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States
DOI
https://doi.org/10.3389/fneur.2020.00181
Journal volume & issue
Vol. 11
Abstract
Read online
No abstracts available.
Keywords
skeletal muscle
channelopathy
sodium channel
NaV1.4
myotonia
voltage-clamp
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