Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia()

مواد مشابهة

• The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome
  بواسطة: McDonell, Laura M, وآخرون
  منشور في: (2014)
• Concordance between whole‐exome sequencing and clinical Sanger sequencing: implications for patient care
  بواسطة: Hamilton, Alison, وآخرون
  منشور في: (2016)
• Exome Sequencing as a Diagnostic Tool for Pediatric-Onset Ataxia
  بواسطة: Sawyer, Sarah L, وآخرون
  منشور في: (2014)
• Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease
  بواسطة: McMillan, Hugh J, وآخرون
  منشور في: (2014)
• Junctional Ectopic Tachycardia
  بواسطة: Francis, Johnson
  منشور في: (2010)