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

Samankaltaisia teoksia

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