On the many faces of Leber hereditary optic neuropathy

Author:

Oostra R.J.,Tijmes N.T.,Cobben J.M.,Boihuis P.A.,Nesselrooij B.P.M.,Houtman W.A.,Kok-Nazaruk M.M.,Bleeker-Wagemakers E.M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 NDI mutation;Black;Eye,1995

2. Rapid shift in genotype of human mitochondrial DNA in a family with Leber's hereditary optic neuropathy;Bolhuis;Biochem Biophys Res Commun,1990

3. Mitochondrial DNA Complex I and III mutations associated with Leber's hereditary optic neuropathy;Brown;Genetics,1992

4. Leber hereditary optic neuropathy: identification of the same mitochondrial NDI mutation in six pedigrees;Howell;Am J Hum Genet,1991

5. When does bilateral optic atrophy become Leber hereditary optic neuropathy;Howell;Am J Hum Genet,1993

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