Ophthalmologic Findings in Leber Hereditary Optic Neuropathy, with Special Reference to mtDNA Mutations

Author:

Nikoskelainen Eeva K.,Huoponen Kirsi,Juvonen Vesa,Lamminen Tarja,Nummelin Kari,Savontaus Marja-Liisa

Publisher

Elsevier BV

Subject

Ophthalmology

Reference35 articles.

1. Primary LHON mutations: trying to separate “fruyt” from “chaff”;Howell;Clin Neurosci,1994

2. When does bilateral optic atrophy become Leber hereditary optic neuropathy [letter]?;Howell;Am J Hum Genet,1993

3. The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy;Huoponen;Hum Genet,1993

4. Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome;Oostra;J Med Genet,1994

5. The clinical features of Leber hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation;Riordan-Eva;Brain,1995

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