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

Podobne zapisy

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