The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
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Zhu, Z., Yao, J., Johns, T., Fu, K., Bie, I. D., Macmillan, C., Cuthbert, A. P., Newbold, R. F., Wang, J.-C., Chevrette, M., et al. (1998) · Nature Genetics · doi:10.1038/3804 · Cited by 623
Mutations of SURF-1 in Leigh Disease Associated with Cytochrome c Oxidase Deficiency
Tiranti, V., Hoertnagel, K., Carrozzo, R., Galimberti, C., Munaro, M., Granatiero, M., Zelante, L., Gasparini, P., Marzella, R., Rocchi, M., et al. (1998) · The American Journal of Human Genetics · doi:10.1086/302150 · Cited by 529
Characterization of , a Yeast Gene Involved in Copper Metabolism and Assembly of Cytochrome Oxidase
Glerum, D. M., Shtanko, A., & Tzagoloff, A. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.24.14504 · Cited by 497
Self-citationCYTOCHROME C OXIDASE: Structure and Spectroscopy
Michel, H., Behr, J., Harrenga, A., & Kannt, A. (1998) · Annual Review of Biophysics and Biomolecular Structure · doi:10.1146/annurev.biophys.27.1.329 · Cited by 450
Mitochondrial DNA Mutations and Pathogenesis
Schon, E. A., Bonilla, E., & DiMauro, S. (1997) · Journal of Bioenergetics and Biomembranes · doi:10.1023/a:1022685929755 · Cited by 424
Self-citationCytochrome c oxidase deficiency in leigh syndrome
DiMauro, S., Servidei, S., Zeviani, M., DiRocco, M., DeVivo, D. C., DiDonato, S., Uziel, G., Berry, K., Hoganson, G., Johnsen, S. D., et al. (1987) · Annals of Neurology · doi:10.1002/ana.410220409 · Cited by 362
Self-citationGlerum, D. M., Shtanko, A., & Tzagoloff, A. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.34.20531 · Cited by 323
Self-citationBenign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency
DiMauro, S., Nicholson, J. F., Hays, A. P., B, A. B., Papadimitriou, A., Koenigsberger, R., & Vivo, D. C. D. (1983) · Annals of Neurology · doi:10.1002/ana.410140209 · Cited by 227
Self-citationFatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome‐c‐oxidase deficiency
DiMauro, S., Mendell, J. R., Sahenk, Z., Bachman, D., Scarpa, A., Scofield, R. M., & Reiner, C. B. (1980) · Neurology · doi:10.1212/wnl.30.8.795 · Cited by 200
Self-citation[43]Cytochemistry and immunocytochemistry of mitochondria in tissue sections
Sciacco, M., & Bonilla, E. (1996) · Methods in Enzymology · doi:10.1016/s0076-6879(96)64045-2 · Cited by 189
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Matoba, S., Kang, J.-G., Patino, W. D., Wragg, A., Boehm, M., Gavrilova, O., Hurley, P. J., Bunz, F., & Hwang, P. M. (2006) · Science · doi:10.1126/science.1126863 · Cited by 1,650
Mitochondrial DNA mutations in human colonic crypt stem cells
Taylor, R. W., Barron, M. J., Borthwick, G. M., Gospel, A., Chinnery, P. F., Samuels, D. C., Taylor, G. A., Plusa, S. M., Needham, S. J., Greaves, L. C., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci19435 · Cited by 530
A role for mitochondrial enzymes in inherited neoplasia and beyond
Eng, C., Kiuru, M., Fernandez, M. J., & Aaltonen, L. A. (2003) · Nature Reviews Cancer · doi:10.1038/nrc1013 · Cited by 392
NAD+-Dependent Activation of Sirt1 Corrects the Phenotype in a Mouse Model of Mitochondrial Disease
Cerutti, R., Pirinen, E., Lamperti, C., Marchet, S., Sauve, A. A., Li, W., Leoni, V., Schon, E. A., Dantzer, F., Auwerx, J., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.04.001 · Cited by 343
Self-citationMitochondrial copper metabolism and delivery to cytochrome c oxidase
Horn, D., & Barrientos, A. (2008) · IUBMB Life · doi:10.1002/iub.50 · Cited by 283
Metadata
- Authors
- Papadopoulou, L. C., Sue, C. M., Davidson, M. M., Tanji, K., Nishino, I., Sadlock, J. E., Krishna, S., Walker, W., Selby, J., Glerum, D. M., Coster, R. V., Lyon, G., Scalais, E., Lebel, R., Kaplan, P., Shanske, S., De Vivo, D. C., Bonilla, E., Hirano, M., DiMauro, S., & Schon, E. A.
- Venue
- Nature Genetics
- Published
- 1999-11
- Volume
- 23
- Issue
- 3
- Pages
- 333-337
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1607363557
- Cited by
- 573
- References
- 26
- FWCI
- 11.96
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene. https://app.cochat.ai/papers/10.1038/15513
- The paper
- Papadopoulou, L. C., Sue, C. M., Davidson, M. M., Tanji, K., Nishino, I., Sadlock, J. E., Krishna, S., Walker, W., Selby, J., Glerum, D. M., Coster, R. V., Lyon, G., Scalais, E., Lebel, R., Kaplan, P., Shanske, S., De Vivo, D. C., Bonilla, E., Hirano, M., . . . Schon, E. A. (1999). Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene. Nature Genetics. https://doi.org/10.1038/15513
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
