J Neuroophthalmol. 2002 Dec;22(4):257-61.

From genotype to phenotype in Leber hereditary optic neuropathy: still more questions than answers.

Newman NJ.

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Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutations. [J Neuroophthalmol. 2002]
Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutations.Howell N, Miller NR, Mackey DA, Arnold A, Herrnstadt C, Williams IM, Kubacka I. J Neuroophthalmol. 2002 Dec; 22(4):262-9.

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Review The genetics of leber hereditary optic neuropathy--prototype of an inherited optic neuropathy with mitochondrial dysfunction. [Semin Ophthalmol. 2008]
Review The genetics of leber hereditary optic neuropathy--prototype of an inherited optic neuropathy with mitochondrial dysfunction.
Eichhorn-Mulligan K, Cestari DM. Semin Ophthalmol. 2008 Jan-Feb; 23(1):27-37.
Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy. [J Med Genet. 2003]
Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy.
Taylor RW, Jobling MS, Turnbull DM, Chinnery PF. J Med Genet. 2003 Jul; 40(7):e85.
[A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis]. [Neurol Neurochir Pol. 2003]
[A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis].
Lubos L, Wajgt A, Maciejowski M, Mroczek-Tońska K, Bartnik E, Dziekanowska D. Neurol Neurochir Pol. 2003 Jan-Feb; 37(1):229-34.
Review [Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype]. [Neurol Neurochir Pol. 2003]
Review [Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype].
Jamrozik Z, Tutaj A, Piechowski-Jóźwiak B, Mroczek-Tońska K, Bartnik E, Kwieciński H. Neurol Neurochir Pol. 2003 May-Jun; 37(3):713-20.
A patient with two mitochondrial DNA mutations causing PEO and LHON. [Eur J Med Genet. 2009]
A patient with two mitochondrial DNA mutations causing PEO and LHON.
Melberg A, Moslemi AR, Palm O, Raininko R, Stålberg E, Oldfors A. Eur J Med Genet. 2009 Jan-Feb; 52(1):47-8. Epub 2008 Nov 5.

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Cited by 6 PubMed Central articles

Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy. [Mol Vis. 2012]
Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy.
Kumar M, Kaur P, Kumar M, Saxena R, Sharma P, Dada R. Mol Vis. 2012; 18:2687-99. Epub 2012 Nov 12.
Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy. [Mol Vis. 2011]
Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy.
Amaral-Fernandes MS, Marcondes AM, Miranda PM, Maciel-Guerra AT, Sartorato EL. Mol Vis. 2011; 17:3175-9. Epub 2011 Dec 7.
Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese. [Mol Vis. 2010]
Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese.
Ji Y, Jia X, Li S, Xiao X, Guo X, Zhang Q. Mol Vis. 2010 Mar 11; 16:416-24. Epub 2010 Mar 11.

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From genotype to phenotype in Leber hereditary optic neuropathy: still more questions than answers.

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