South Asian-specific MYBPC3(Δ25bp) Intronic Deletion and its role in Cardiomyopathies and Heart Failure

مواد مشابهة

• Association of Cardiomyopathy With MYBPC3 D389V and MYBPC3(Δ25bp)Intronic Deletion in South Asian Descendants
  بواسطة: Viswanathan, Shiv Kumar, وآخرون
  منشور في: (2018)
• Reevaluation of the South Asian MYBPC3(Δ25bp) Intronic Deletion in Hypertrophic Cardiomyopathy
  بواسطة: Harper, Andrew R., وآخرون
  منشور في: (2020)
• Genetic, clinical, molecular, and pathogenic aspects of the South Asian–specific polymorphic MYBPC3(Δ25bp) variant
  بواسطة: Arif, Mohammed, وآخرون
  منشور في: (2020)
• MYBPC3's alternate ending: consequences and therapeutic implications of a highly prevalent 25 bp deletion mutation
  بواسطة: Kuster, Diederik W. D., وآخرون
  منشور في: (2013)
• A Hypertrophic Cardiomyopathy-associated MYBPC3 Mutation Common in Populations of South Asian Descent Causes Contractile Dysfunction
  بواسطة: Kuster, Diederik W. D., وآخرون
  منشور في: (2015)