α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current

Gelijkaardige items

• LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype
  door: Cheng, Jianding, et al.
  Gepubliceerd in: (2011)
• Sudden Infant Death Syndrome-Associated Mutations in the Sodium Channel Beta Subunits
  door: Tan, Bi-Hua, et al.
  Gepubliceerd in: (2010)
• Syntrophin mutation associated with long QT syndrome through activation of the nNOS–SCN5A macromolecular complex
  door: Ueda, Kazuo, et al.
  Gepubliceerd in: (2008)
• The common African American polymorphism SCN5A-S1103Y interacts with mutation SCN5A-R680H to increase late Na current
  door: Cheng, Jianding, et al.
  Gepubliceerd in: (2011)
• A Novel Mechanism for Sudden Infant Death Syndrome (SIDS): Persistent Late Sodium Current Secondary to Mutations in Caveolin-3
  door: Cronk, Lisa B., et al.
  Gepubliceerd in: (2006)