A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis-Reference-Cited by-同舟云学术

A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis

Published:2015-12-11 Issue:2 Volume:86 Page:161-169
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Habbout Karima,Poulin Hugo,Rivier François,Giuliano Serena,Sternberg Damien,Fontaine Bertrand,Eymard Bruno,Morales Raul Juntas,Echenne Bernard,King Louise,Hanna Michael G.,Männikkö Roope,Chahine Mohamed,Nicole Sophie,Bendahhou Said

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference33 articles.

1. Muscle channelopathies and related diseases

2. Sodium channelopathies of skeletal muscle result from gain or loss of function

3. PATHOMECHANISMS IN CHANNELOPATHIES OF SKELETAL MUSCLE AND BRAIN

4. Congenital Myasthenic Syndromes: Multiple Molecular Targets at the Neuromuscular Junction

5. Congenital myasthenic syndromes

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