scholarly journals Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A

Brain ◽  
2001 ◽  
Vol 124 (6) ◽  
pp. 1091-1099 ◽  
Author(s):  
D. Sternberg
Keyword(s):  
Sodium Channel ◽  
Periodic Paralysis ◽  
Channel Gene ◽  
Sodium Channel Gene ◽  
Hypokalaemic Periodic Paralysis

Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene

1991 ◽  
Vol 30 (6) ◽  
pp. 810-816 ◽  
Author(s):  
G. C. Ebers ◽  
A. L. George ◽  
R. L. Barchi ◽  
S. S. Ting-Passador ◽  
R. G. Kallen ◽  
...  
Keyword(s):  
Sodium Channel ◽  
Periodic Paralysis ◽  
Hyperkalemic Periodic Paralysis ◽  
Paramyotonia Congenita ◽  
Channel Gene ◽  
Adult Muscle ◽  
Sodium Channel Gene

Severe myotonia in juvenile myotonic dystrophy type 2 and sodium channel gene mutation

2013 ◽  
Vol 333 ◽  
pp. e456
Author(s):  
E. Bugiardini ◽  
A. Soriano Caminero ◽  
R. Cardani ◽  
A. Botta ◽  
M.P. Wicklund ◽  
...  
Keyword(s):  
Sodium Channel ◽  
Myotonic Dystrophy ◽  
Gene Mutation ◽  
Myotonic Dystrophy Type ◽  
Myotonic Dystrophy Type 2 ◽  
Channel Gene ◽  
Sodium Channel Gene

Sodium channel gene mutations in hypokalemic periodic paralysis: An uncommon cause in the UK

Neurology ◽  
2001 ◽  
Vol 57 (7) ◽  
pp. 1323-1325 ◽  
Author(s):  
N. P. Davies ◽  
L. H. Eunson ◽  
M. Samuel ◽  
M. G. Hanna
Keyword(s):  
Sodium Channel ◽  
Gene Mutations ◽  
Periodic Paralysis ◽  
Hypokalemic Periodic Paralysis ◽  
Channel Gene ◽  
Sodium Channel Gene ◽  
The Uk

Identification of a Thr-to-Met Mutation in the Skeletal Muscle Sodium Channel Gene in Hyperkalemic Periodic Paralysis of a Japanese Family

1993 ◽  
Vol 707 (1 Molecular Bas) ◽  
pp. 342-345
Author(s):  
KIICHI ARAHATA ◽  
JIANZHOU WANG ◽  
W. GREGORY FEERO ◽  
HIROSHI HAYAKAWA ◽  
KOICHI HONDA ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Sodium Channel ◽  
Periodic Paralysis ◽  
Hyperkalemic Periodic Paralysis ◽  
Japanese Family ◽  
Channel Gene ◽  
Sodium Channel Gene
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