Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in <i>SCN4A</i>.

Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A.

Elia, Nathaniel; Nault, Trystan; McMillan, Hugh J; Graham, Gail E; Huang, Lijia; Cannon, Stephen C.

Afiliação

Elia N; Department of Physiology, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Nault T; Molecular, Cellular, and Integrative Physiology Program, UCLA, Los Angeles, CA, United States.
McMillan HJ; Division of Neurology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada.
Graham GE; Division of Neurology, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada.
Huang L; Department of Genetics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada.
Cannon SC; Department of Genetics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON, Canada.

Front Neurol ; 11: 181, 2020.

Article em En | MEDLINE | ID: mdl-32265824