Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy.

समान संसाधन

• Double mutations in CIS can confound genotype-phenotype correlations in hypertrophic cardiomyopathy
  द्वारा: Blair, E, और अन्य
  प्रकाशित: (2000)
• Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.
  द्वारा: Blair, E, और अन्य
  प्रकाशित: (2003)
• A Genotype-phenotype Taxonomy of Hypertrophic Cardiomyopathy
  द्वारा: Lara Curran, BSc, और अन्य
  प्रकाशित: (2024-01-01)
• A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
  द्वारा: Carballo, S, और अन्य
  प्रकाशित: (2004)
• Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
  द्वारा: Blair, E, और अन्य
  प्रकाशित: (2002)