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2005 | 1 |
2006 | 1 |
2008 | 1 |
2025 | 0 |
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OPA1 mutations and mitochondrial DNA haplotypes in autosomal dominant optic atrophy.
Genet Med. 2006 Apr;8(4):217-25. doi: 10.1097/01.gim.0000214299.61930.c0.
Genet Med. 2006.
PMID: 16617242
Free article.
Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy.
Mayorov VI, Lowrey AJ, Biousse V, Newman NJ, Cline SD, Brown MD.
Mayorov VI, et al.
BMC Biochem. 2008 Sep 10;9:22. doi: 10.1186/1471-2091-9-22.
BMC Biochem. 2008.
PMID: 18783614
Free PMC article.
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The role of the ND5 gene in LHON: characterization of a new, heteroplasmic LHON mutation.
Mayorov V, Biousse V, Newman NJ, Brown MD.
Mayorov V, et al.
Ann Neurol. 2005 Nov;58(5):807-11. doi: 10.1002/ana.20669.
Ann Neurol. 2005.
PMID: 16240359
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