Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese

Gelijkaardige items

• Mitochondrial DNA Haplogroups M7b1′2 and M8a Affect Clinical Expression of Leber Hereditary Optic Neuropathy in Chinese Families with the m.11778G→A Mutation
  door: Ji, Yanli, et al.
  Gepubliceerd in: (2008)
• An atypical Leber's hereditary optic neuropathy with the 11778 mutation.
  door: Hotta, Y, et al.
  Gepubliceerd in: (1993)
• Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy
  door: Chen, Yabin, et al.
  Gepubliceerd in: (2013)
• Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients
  door: Zhang, A-Mei, et al.
  Gepubliceerd in: (2012)
• A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
  door: Sadun, Alfredo A, et al.
  Gepubliceerd in: (2002)