Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation

This publication has 28 references indexed in Scilit:

• Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.
  Journal of Medical Genetics, 1994
• The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy
  Human Genetics, 1993
• Reevaluation of the linkage of an optic atrophy susceptibility gene to X-chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON)
  1993
• The two locus control of Leber hereditary optic neurophathy and a high penetrance in Japanese pedigrees
  Human Genetics, 1993
• Mitochondrial DNA Analysis as a Diagnostic Tool in Singleton Cases of Leber's Hereditary Optic Neuropathy
  Ophthalmic Paediatrics and Genetics, 1993
• An ND-6 mitochondrial DNA mutation associated with leber hereditary optic neuropathy
  Biochemical and Biophysical Research Communications, 1992
• Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation.
  1991
• Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy
  Biochemical and Biophysical Research Communications, 1991
• SEGREGATION OF MITOCHONDRIAL GENOMES IN A HETEROPLASMIC LINEAGE WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY
  1990
• Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy
  Science, 1988