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long QT syndrome type 1 (LQT1, Romano-Ward syndrome)
Genetics: - autosomal dominant - associated with defects in KCNQ1Interactions
disease interactionsRelated
Jervell & Lange-Nielsen syndromeGeneral
long QT syndromeDatabase Correlations
OMIM 192500References
- UpToDate 14.1 http://www.utdol.com
- OMIM :accession 192500