Long QT Syndrome

From ECGpedia
Revision as of 08:02, 15 May 2007 by Drj (talk | contribs) (New page: Conclusions—This genotype–phenotype study indicates that in type-1 LQTS, mutations located in the transmembrane portion of the ion channel protein and the degree of ion channel dysfu...)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.


Conclusions—This genotype–phenotype study indicates that in type-1 LQTS, mutations located in the transmembrane portion of the ion channel protein and the degree of ion channel dysfunction caused by the mutations are important independent risk factors influencing the clinical course of this disorder.[1]

References

  1. []
Retrieved from "https://en.ecgpedia.org/index.php?title=Long_QT_Syndrome&oldid=1824"