Loss-of-Function Mutations in the KCNJ8-Encoded Kir6.1 K(ATP) Channel and Sudden Infant Death Syndrome

Eitemau Tebyg

• Gain-of-Function Mutation, S422L, in the KCNJ8-Encoded Cardiac K(ATP) Channel Kir6.1 as a Pathogenic Substrate for J Wave Syndromes
  gan: Medeiros-Domingo, Argelia, et al.
  Cyhoeddwyd: (2010)
• Sudden Infant Death Syndrome-Associated Mutations in the Sodium Channel Beta Subunits
  gan: Tan, Bi-Hua, et al.
  Cyhoeddwyd: (2010)
• Cardiac Channel Molecular Autopsy: Insights From 173 Consecutive Cases of Autopsy-Negative Sudden Unexplained Death Referred for Postmortem Genetic Testing
  gan: Tester, David J., et al.
  Cyhoeddwyd: (2012)
• α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current
  gan: Cheng, Jianding, et al.
  Cyhoeddwyd: (2009)
• Kir6.1-dependent K(ATP) channels in lymphatic smooth muscle and vessel dysfunction in mice with Kir6.1 gain-of-function
  gan: Davis, Michael J., et al.
  Cyhoeddwyd: (2020)