|
Volumn 80, Issue 16, 2013, Pages 1472-1475
|
Prevalence study of genetically defined skeletal muscle channelopathies in England
|
Author keywords
[No Author keywords available]
|
Indexed keywords
INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR2.1;
SODIUM CHANNEL NAV1.4;
UNCLASSIFIED DRUG;
VOLTAGE GATED CHLORIDE CHANNEL;
VOLTAGE GATED CHLORIDE CHANNEL 1;
CHLORIDE CHANNEL;
CLC 1 CHANNEL;
CLC-1 CHANNEL;
INWARDLY RECTIFYING POTASSIUM CHANNEL;
KCNJ2 PROTEIN, HUMAN;
SCN4A PROTEIN, HUMAN;
SODIUM CHANNEL;
ADULT;
ANDERSEN SYNDROME;
ARTICLE;
CLINICAL STUDY;
DEMOGRAPHY;
DISEASE ASSOCIATION;
ELECTROPHYSIOLOGY;
FAMILY HISTORY;
FEMALE;
GENE MUTATION;
GENOTYPE;
HETEROZYGOTE;
HOMOZYGOTE;
HUMAN;
INHERITANCE;
MAJOR CLINICAL STUDY;
MALE;
MUSCLE CHANNELOPATHY;
MYOTONIA;
NONDYSTROPHIC MYOTONIA;
PERIODIC PARALYSIS;
PREVALENCE;
PRIORITY JOURNAL;
THOMSEN DISEASE;
UNITED KINGDOM;
CHANNELOPATHY;
GENETIC DATABASE;
GENETICS;
HYPOKALEMIC PERIODIC PARALYSIS;
MIDDLE AGED;
MUSCLE DISEASE;
MUTATION;
PHYSIOLOGY;
SKELETAL MUSCLE;
STATISTICAL ANALYSIS;
ADULT;
CHANNELOPATHIES;
CHLORIDE CHANNELS;
DATA INTERPRETATION, STATISTICAL;
DATABASES, GENETIC;
ENGLAND;
FEMALE;
GREAT BRITAIN;
HUMANS;
HYPOKALEMIC PERIODIC PARALYSIS;
MALE;
MIDDLE AGED;
MUSCLE, SKELETAL;
MUSCULAR DISEASES;
MUTATION;
MYOTONIA;
MYOTONIC DISORDERS;
NAV1.4 VOLTAGE-GATED SODIUM CHANNEL;
PARALYSES, FAMILIAL PERIODIC;
PARALYSIS, HYPERKALEMIC PERIODIC;
POTASSIUM CHANNELS, INWARDLY RECTIFYING;
PREVALENCE;
SODIUM CHANNELS;
|
EID: 85047688777
PISSN: 00283878
EISSN: 1526632X
Source Type: Journal
DOI: 10.1212/WNL.0b013e31828cf8d0 Document Type: Article |
Times cited : (102)
|
References (10)
|