An atypical Leber's hereditary optic neuropathy with the 11778 mutation.

Ítems similars

• Increase of mitochondrial DNA in blood cells of patients with Leber’s hereditary optic neuropathy with 11778 mutation
  per: Yen, M-Y, et al.
  Publicat: (2002)
• Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases
  per: Carelli, V, et al.
  Publicat: (2001)
• A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
  per: Sadun, Alfredo A, et al.
  Publicat: (2002)
• Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy
  per: Miyaue, Noriyuki, et al.
  Publicat: (2019)
• Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
  per: Brown, M D, et al.
  Publicat: (1997)