Low-Penetrance Branches in Matrilineal Pedigrees with Leber Hereditary Optic Neuropathy

This publication has 17 references indexed in Scilit:

• Reply to Hofmann et al.
  The American Journal of Human Genetics, 1998
• mtDNA Mutations That Cause Optic Neuropathy: How Do We Know?
  The American Journal of Human Genetics, 1998
• Leber hereditary optic neuropathy: Mitochondrial mutations and degeneration of the optic nerve
  Vision Research, 1997
• Tissue distribution of the ND4/11778 mutation in heteroplasmic lineages with Leber hereditary optic neuropathy
  Human Mutation, 1997
• The mitochondrial DNA transfer RNA ^Leu(UUR) A→G(3243) mutation: A clinical and genetic study
  Brain, 1995
• The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
  Brain, 1995
• Leber hereditary optic neuropathy in Australia
  Australian and New Zealand Journal of Ophthalmology, 1992
• Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy
  Biochemical and Biophysical Research Communications, 1991
• Sequence and organization of the human mitochondrial genome
  Nature, 1981
• Ueber hereditäre und congenital-angelegte Sehnervenleiden
  Graefe's Archive for Clinical and Experimental Ophthalmology, 1871