An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.

Míreanna Comhchosúla

• A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia.
  le: Kaukonen, J, et al.
  Foilsithe: (1999)
• Mitochondrial DNA inheritance in patients with deleted mtDNA
  le: Quintana-Murci, L., et al.
  Foilsithe: (2001)
• The mutation rate of the human mtDNA deletion mtDNA4977.
  le: Shenkar, R., et al.
  Foilsithe: (1996)
• A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions
  le: Tyynismaa, Henna, et al.
  Foilsithe: (2009)
• Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion.
  le: Barrientos, A., et al.
  Foilsithe: (1996)