Congenital Long QT Syndrome and 2:1 Atrioventricular Block with a Mutation of the SCN5A Gene View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2003-01

AUTHORS

M. Miura, H. Yamagishi, Y. Morikawa, R. Matsuoka

ABSTRACT

Infants with congenital long QT syndrome (LQTS) and 2:1 atrioventricular block (AVB) have been recognized as a clinical subset of children with LQTS. However, the genotype of this disorder is not well-known. We report an infant with LQTS and 2:1 AVB with a mutation of the SCN5A gene (LQT3). In some patients with LQTS and 2:1 AVB, the disorder may be due to mutation of the SCN5A gene (LQT3). More... »

PAGES

70-72

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00246-002-0169-5

DOI

http://dx.doi.org/10.1007/s00246-002-0169-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1046296298

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/12574983


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