Further evidence for genetic heterogeneity of autosomal dominant disorders with accumulation of multiple deletions of mitochondrial DNA

Similar Items

• Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritance
  by: Hall, C, et al.
  Published: (2002)
• Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.
  by: Cormier, V, et al.
  Published: (1991)
• Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.
  by: Zeviani, M, et al.
  Published: (1990)
• Evidence for Locus Heterogeneity in Autosomal Dominant Limb-Girdle Muscular Dystrophy
  by: Speer, Marcy C., et al.
  Published: (1995)
• Autosomal dominant retinitis pigmentosa: no evidence for nonallelic genetic heterogeneity on 3q.
  by: Kumar-Singh, R, et al.
  Published: (1993)