Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy.

Author:

Nikoskelainen E K,Marttila R J,Huoponen K,Juvonen V,Lamminen T,Sonninen P,Savontaus M L

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference40 articles.

1. The spectrum of mitochondrial DNA mutations in families withLeber hereditary optic neuroretinopathy;Huoponen, K.; Lamminen, T.; Juvonen, V.; Aula, P.; Nikoskelainen, E.; Savontaus, M.-L.;Hum Genet,1993

2. Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene;Howell, N.; Kubacka, J.; Halvorsson, S.; Mackey, D.;Genetics,1993

3. Cytochrome b mutations in Leber hereditary optic neuropathy;Johns, D.R.; Neufeld, M.J.;Biochem Biophys Res Commun,1991

4. An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy;Johns, D.R.; NeufeldMJ, Park; R.D.;Biochem Biophys Res Commun,1992

5. A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology. Am.7 Hum Genet;Mackey, D.; Howell, N.,1992

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