Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy

Gelijkaardige items

• Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese
  door: Ji, Yanli, et al.
  Gepubliceerd in: (2010)
• Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy
  door: Li, Yadi, et al.
  Gepubliceerd in: (2017)
• 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 recurrent mutation in GUCY2D associated with autosomal dominant cone dystrophy in a Chinese family
  door: Xiao, Xueshan, et al.
  Gepubliceerd in: (2011)
• 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)