X-chromosomal gene in Leber hereditary optic neuroretinopathy.

Podobne zapisy

• Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7.
  od: Vilkki, J, i wsp.
  Wydane: (1991)
• Reevaluation of the linkage of an optic atrophy susceptibility gene to X-chromosomal markers in Finnish families with Leber hereditary optic neuroretinopathy (LHON)
  od: Juvonen, V, i wsp.
  Wydane: (1993)
• mtDNA heteroplasmy in Leber hereditary optic neuroretinopathy.
  od: Cormier, V, i wsp.
  Wydane: (1991)
• A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy.
  od: Huoponen, K, i wsp.
  Wydane: (1991)
• X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation.
  od: Bu, X D, i wsp.
  Wydane: (1991)