Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4-Reference-Cited by-同舟云学术

Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4

Published:2020-04-29 Issue: Volume:11 Page:
ISSN:1664-2295
Container-title:Frontiers in Neurology
language:
Short-container-title:Front. Neurol.

Author:

Pagliarani Serena,Lucchiari Sabrina,Scarlato Marina,Redaelli Elisa,Modoni Anna,Magri Francesca,Fossati Barbara,Previtali Stefano C.,Sansone Valeria A.,Lecchi Marzia,Lo Monaco Mauro,Meola Giovanni,Comi Giacomo P.

Publisher

Frontiers Media SA

Subject

Neurology (clinical),Neurology

Reference18 articles.

1. The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment;Matthews;Brain,2010

2. Sodium channelopathies of skeletal muscle;Cannon,2017

3. Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study;Männikkö;Lancet,2018

4. Muscle channelopathies: recent advances in genetics, pathophysiology and therapy;Suetterlin;Curr Opin Neurol,2014

5. Severe neonatal episodic laryngospasm due to de novo SCN4A mutations;Lion-François;Neurology,2010

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3. Diagnostics in skeletal muscle channelopathies;Expert Review of Molecular Diagnostics;2023-11-29

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5. Cannabidiol Selectively Binds to the Voltage-Gated Sodium Channel Nav1.4 in Its Slow-Inactivated State and Inhibits Sodium Current;Biomedicines;2021-09-02