A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia.

Míreanna Comhchosúla

• An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.
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  Foilsithe: (1996)
• A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions
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  Foilsithe: (2009)
• Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling
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  Foilsithe: (2009)
• Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM).
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  Foilsithe: (1998)
• Two families with autosomal dominant progressive external ophthalmoplegia
  le: Kiechl, S, et al.
  Foilsithe: (2004)