| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/BRAIN/123.9.1896 |
| P698 | PubMed publication ID | 10960053 |
| P2093 | author name string | P Cortelli | |
| P Montagna | |||
| S Cevoli | |||
| R Lodi | |||
| B Barbiroli | |||
| V Carelli | |||
| S Iotti | |||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | hereditary optic neuropathy | Q55789244 |
| mitochondrion | Q39572 | ||
| mitochondrial DNA | Q27075 | ||
| P304 | page(s) | 1896-1902 | |
| P577 | publication date | 2000-09-01 | |
| P1433 | published in | Brain | Q897386 |
| P1476 | title | 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation | |
| P478 | volume | 123 ( Pt 9) |
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| Q47136745 | Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population |
| Q34507282 | Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees. |
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| Q42037621 | The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype |
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