| scholarly article | Q13442814 |
| P8978 | DBLP publication ID | journals/nar/ScharfeZHJKDLPGNMM00 |
| P356 | DOI | 10.1093/NAR/28.1.155 |
| P932 | PMC publication ID | 102491 |
| P698 | PubMed publication ID | 10592209 |
| P5875 | ResearchGate publication ID | 220582186 |
| P50 | author | Thomas Meitinger | Q28039310 |
| P2093 | author name string | Lill R | |
| Neupert W | |||
| Gerbitz KD | |||
| Jaksch M | |||
| Klopstock T | |||
| Scharfe C | |||
| Mewes HW | |||
| Prokisch H | |||
| Dembowski M | |||
| Zaccaria P | |||
| Hoertnagel K | |||
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| A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy | Q33681493 | ||
| Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency | Q34388122 | ||
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| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | database | Q8513 |
| P304 | page(s) | 155-158 | |
| P577 | publication date | 2000-01-01 | |
| P1433 | published in | Nucleic Acids Research | Q135122 |
| P1476 | title | MITOP, the mitochondrial proteome database: 2000 update | |
| P478 | volume | 28 |
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