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Novel deletion mutation in the cardiac sodium channel inactivation gate causes long QT syndrome.

AuthorsNicola Detta, Giulia Frisso, Alberto Zullo, Berardo Sarubbi, Carla Cozzolino, Emanuele Romeo, Dao W Wang, Raffaele Calabrò, Francesco Salvatore, Alfred L George Jr
JournalInternational journal of cardiology (Int J Cardiol) Vol. 165 Issue 2 Pg. 362-5 (May 10 2013) ISSN: 1874-1754 [Electronic] Netherlands
PMID22980924 (Publication Type: Letter)
Chemical References
  • NAV1.5 Voltage-Gated Sodium Channel
  • SCN5A protein, human
Topics
  • Adult
  • Amino Acid Sequence
  • Female
  • Follow-Up Studies
  • Humans
  • Long QT Syndrome (diagnosis, genetics)
  • Male
  • NAV1.5 Voltage-Gated Sodium Channel (genetics)
  • Pedigree
  • Sequence Deletion (genetics)

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