Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Non-Synonymous Single Nucleotide Variants in Type 1 and 2 Long QT Syndrome

مواد مشابهة

• Classification and Reporting of Potentially Pro-Arrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing
  بواسطة: Giudicessi, John R., وآخرون
  منشور في: (2018)
• The genetic architecture of long QT syndrome: A critical reappraisal
  بواسطة: Giudicessi, John R., وآخرون
  منشور في: (2018)
• Enhanced Classification of Brugada Syndrome–Associated and Long-QT Syndrome–Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium Channel
  بواسطة: Kapplinger, Jamie D., وآخرون
  منشور في: (2015)
• Enhancing the Predictive Power of Mutations in the C-Terminus of the KCNQ1-Encoded Kv7.1 Voltage-Gated Potassium Channel
  بواسطة: Kapplinger, Jamie D., وآخرون
  منشور في: (2015)
• Genetic Testing for Long QT Syndrome - Distinguishing Pathogenic Mutations from Benign Variants
  بواسطة: Kapa, Suraj, وآخرون
  منشور في: (2009)