Mutations atKCNQ1and an unknown locus cause long QT syndrome in a large Australian family: Implications for genetic testing
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33274/fullpdf
Reference44 articles.
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3. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization;Arking;Nat Genet,2006
4. A candidate locus approach identifies a long QT syndrome gene mutation;Beery;Biol Res Nurs,2003
5. Mutation of an A-kinase-anchoring protein causes long-QT syndrome;Chen;Proc Natl Acad Sci USA,2007
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