Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene

Documenti analoghi

• Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice
  di: McConnell, Bradley K., et al.
  Pubblicazione: (1999)
• Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice
  di: McConnell, Bradley K., et al.
  Pubblicazione: (1999)
• Cell-Intrinsic Functional Effects of the α-Cardiac Myosin Arg-403-Gln Mutation in Familial Hypertrophic Cardiomyopathy
  di: Chuan, Peiying, et al.
  Pubblicazione: (2012)
• The cardiac myosin heavy chain Arg-403-->Gln mutation that causes hypertrophic cardiomyopathy does not affect the actin- or ATP-binding capacities of two size-limited recombinant myosin heavy chain fragments.
  di: Eldin, P, et al.
  Pubblicazione: (1995)
• Development of induced pluripotent stem cells from a patient with hypertrophic cardiomyopathy who carries the pathogenic myosin heavy chain 7 mutation p.Arg403Gln
  di: Mira Holliday, et al.
  Pubblicazione: (2018-12-01)