Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation

समान संसाधन

• Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene
  द्वारा: Deprez, R H Lekanne, और अन्य
  प्रकाशित: (2006)
• Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects
  द्वारा: Wessels, Marja W, और अन्य
  प्रकाशित: (2015)
• Haploinsufficiency of MYBPC3 Exacerbates the Development of Hypertrophic Cardiomyopathy in Heterozygous Mice
  द्वारा: Barefield, David, और अन्य
  प्रकाशित: (2014)
• MYBPC3 truncation mutations enhance actomyosin contractile mechanics in human hypertrophic cardiomyopathy
  द्वारा: O’Lea ry, Thomas S., और अन्य
  प्रकाशित: (2018)
• Non-sustained ventricular tachycardias, conduction disorders and an impaired left ventricular ejection fraction in a 32-year-old woman
  द्वारा: Alsters, S., और अन्य
  प्रकाशित: (2019)