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Novel AKAP9 mutation and long QT syndrome in a patient with torsades des pointes

  • Dario Bottigliero
  • Ilenia Monaco
  • Rosa Santacroce
  • Grazia Casavecchia
  • Michele Correale
  • Francesca Guastafierro
  • Angelica Leccese
  • Giorgia Cordisco
  • Riccardo Ieva
  • Roberta Trunzo
  • Matteo Di Biase
  • Maurizio Margaglione
  • Natale Daniele BrunettiEmail author
Case Reports
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Notes

References

  1. 1.
    de Villiers CP, van der Merwe L, Crotti L, Goosen A, George AL Jr, Schwartz PJ, et al. AKAP9 is a genetic modifier of congenital long-QT syndrome type 1. Circ Cardiovasc Genet. 2014;7:599–606.CrossRefPubMedPubMedCentralGoogle Scholar
  2. 2.
    Chen L, Marquardt ML, Tester DJ, Sampson KJ, Ackerman MJ, Kass RS. Mutation of an A-kinase-anchoring protein causes long-QT syndrome. Proc Natl Acad Sci U S A. 2007;104:20990–5.CrossRefPubMedPubMedCentralGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  • Dario Bottigliero
    • 1
  • Ilenia Monaco
    • 1
  • Rosa Santacroce
    • 1
  • Grazia Casavecchia
    • 1
  • Michele Correale
    • 1
  • Francesca Guastafierro
    • 1
  • Angelica Leccese
    • 1
  • Giorgia Cordisco
    • 1
  • Riccardo Ieva
    • 2
  • Roberta Trunzo
    • 1
  • Matteo Di Biase
    • 3
  • Maurizio Margaglione
    • 1
  • Natale Daniele Brunetti
    • 1
    Email author
  1. 1.Department of Medical & Surgical SciencesUniversity of FoggiaFoggiaItaly
  2. 2.Cardiology DepartmentOspedali Riuniti University HospitalFoggiaItaly
  3. 3.GVM Care & ResearchBariItaly

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