A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia.

Ørstavik, Kristin

A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia. [electronic resource] - Journal of neuromuscular diseases Jun 2015 - 181-184 p. digital

Publication Type: Journal Article

ISSN: 2214-3599

Standard No.: 10.3233/JND-150069 doi

A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia.

APA

Ørstavik K., Wallace S. C., Torbergsen T., Abicht A., Erik Tangsrud S., Kerty E. & Rasmussen M. (2015). A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia. : Journal of neuromuscular diseases.

Chicago

Ørstavik Kristin, Wallace Sean Ciaran, Torbergsen Torberg, Abicht Angela, Erik Tangsrud Svein, Kerty Emilia and Rasmussen Magnhild. 2015. A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia. : Journal of neuromuscular diseases.

Harvard

Ørstavik K., Wallace S. C., Torbergsen T., Abicht A., Erik Tangsrud S., Kerty E. and Rasmussen M. (2015). A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia. : Journal of neuromuscular diseases.

MLA

Ørstavik Kristin, Wallace Sean Ciaran, Torbergsen Torberg, Abicht Angela, Erik Tangsrud Svein, Kerty Emilia and Rasmussen Magnhild. A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia. : Journal of neuromuscular diseases. 2015.

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