(Q50497138)
Statements
1 reference
Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X. (English)
1 reference
Wei J
1 reference
Fish FA
1 reference
Myerburg RJ
1 reference
Roden DM
1 reference
George AL Jr
1 reference
1 April 2000
1 reference
1 reference
15
1 reference
4
1 reference
387-388
1 reference
Identifiers
1 reference