Leber optic neuropathy
Comment on
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Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation.Am J Hum Genet. 1991 May;48(5):935-42. Am J Hum Genet. 1991. PMID: 2018041 Free PMC article.
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An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.Am J Hum Genet. 1990 Oct;47(4):629-34. Am J Hum Genet. 1990. PMID: 2121024 Free PMC article.
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Blindness in offspring of women blinded by Leber's hereditary optic neuropathy.Lancet. 1993 Apr 17;341(8851):1020-1. doi: 10.1016/0140-6736(93)91105-u. Lancet. 1993. PMID: 8096896 No abstract available.
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Leber hereditary optic neuropathy, progressive visual loss, and multiple-sclerosis-like symptoms.Am J Ophthalmol. 2001 Oct;132(4):591-3. doi: 10.1016/s0002-9394(01)01045-5. Am J Ophthalmol. 2001. PMID: 11589893
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Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.Am J Hum Genet. 1994 Aug;55(2):410-2. Am J Hum Genet. 1994. PMID: 8037217 Free PMC article. No abstract available.
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[Hereditary optic atrophies].Rev Neurol (Paris). 2010 Dec;166(12):959-65. doi: 10.1016/j.neurol.2010.07.033. Epub 2010 Nov 5. Rev Neurol (Paris). 2010. PMID: 21056443 Review. French.
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Leber's hereditary optic neuropathy: a genetic disorder of the eye.Insight. 1997 Sep;22(3):94-6. doi: 10.1016/s1060-135x(97)90084-1. Insight. 1997. PMID: 9379083 Review.
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