Title
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations
Author
Faculty/Department
Faculty of Medicine and Health Sciences
Publication type
article
Publication
Leiden ,
Source (journal)
European journal of human genetics / European Society of Human Genetics. - Leiden
Volume/pages
2(1994) , p. 110-124
ISSN
1018-4813
Carrier
E
Target language
English (eng)
Affiliation
University of Antwerp
Handle