Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients

Eitemau Tebyg

• Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy
  gan: Bi, Rui, et al.
  Cyhoeddwyd: (2012)
• Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese
  gan: Ji, Yanli, et al.
  Cyhoeddwyd: (2010)
• Mitochondrial DNA Haplogroups M7b1′2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G→A Mutation
  gan: Ji, Yanli, et al.
  Cyhoeddwyd: (2008)
• Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy
  gan: Chen, Yabin, et al.
  Cyhoeddwyd: (2013)
• Mitochondrial ND-I mutation in Leber hereditary optic neuropathy.
  gan: Johns, D R
  Cyhoeddwyd: (1992)