The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.
Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)
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Citations
Cites
Sequence and organization of the human mitochondrial genome
Anderson, S., Bankier, A. T., Barrell, B. G., de Bruijn, M. H. L., Coulson, A. R., Drouin, J., Eperon, I. C., Nierlich, D. P., Roe, B. A., Sanger, F., et al. (1981) · Nature · doi:10.1038/290457a0 · Cited by 9,636
Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy
Wallace, D. C., Singh, G., Lott, M. T., Hodge, J. A., Schurr, T. G., Lezza, A. M. S., Elsas, L. J., & Nikoskelainen, E. K. (1988) · Science · doi:10.1126/science.3201231 · Cited by 2,440
Principles of Exercise Testing and Interpretation.
(1987) · Annals of Internal Medicine · doi:10.7326/0003-4819-106-4-646 · Cited by 2,359
Goto, Y.-I., Nonaka, I., & Horai, S. (1990) · Nature · doi:10.1038/348651a0 · Cited by 2,070
Shoffner, J. M., Lott, M. T., Lezza, A. M. S., Seibel, P., Ballinger, S. W., & Wallace, D. C. (1990) · Cell · doi:10.1016/0092-8674(90)90059-n · Cited by 1,482
Geisterfer-Lowrance, A. A. T., Kass, S., Tanigawa, G., Vosberg, H.-P., McKenna, W., Seidman, C. E., & Seidman, J. G. (1990) · Cell · doi:10.1016/0092-8674(90)90274-i · Cited by 1,380
Muscle Biopsy: A Practical Approach
Dubowitz, V., Sewry, C. A., Oldfors, A., & Lane, R. J. M. (2020) · Cited by 1,335
A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.
Holt, I. J., Harding, A. E., Petty, R., & MORGAN-HUGHES, J. A. (1990) · PubMed · Cited by 1,005
Muscle Biopsy: A Practical Approach
Bourne, A. J. (1986) · Pathology · doi:10.3109/00313028609059493 · Cited by 576
Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1
Jarcho, J. A., McKenna, W., Pare, J. A. P., Solomon, S. D., Holcombe, R. F., Dickie, S., Levi, T., Donis-Keller, H., Seidman, J. G., & Seidman, C. E. (1989) · New England Journal of Medicine · doi:10.1056/nejm198911163212005 · Cited by 540
Cited by
Inhibition of mitochondrial beta-oxidation as a mechanism of hepatotoxicity
Fromenty, B., & Pessayre, D. (1995) · Pharmacology & Therapeutics · doi:10.1016/0163-7258(95)00012-6 · Cited by 665
King, M. P., Koga, Y., Davidson, M., & Schon, E. A. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.2.480 · Cited by 458
Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
Muntoni, F., Cau, M., Ganau, A., Congiu, R., Arvedi, G., Mateddu, A., Marrosu, M. G., Cianchetti, C., Realdi, G., Cao, A., et al. (1993) · New England Journal of Medicine · doi:10.1056/nejm199309233291304 · Cited by 416
Sproule, D. M., & Kaufmann, P. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1444.011 · Cited by 351
Li, S., Pan, H., Tan, C., Sun, Y., Song, Y., Zhang, X., Yang, W., Wang, X., Li, D., Dai, Y., et al. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.01.013 · Cited by 106
Metadata
- Authors
- Zeviani, M., Gellera, C., Antozzi, C., Rimoldi, M., Morandi, L., Tiranti, V., DiDonato, S., & Villani, F.
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 1991-07
- Volume
- 338
- Issue
- 8760
- Pages
- 143-147
- ISSN
- 0099-5355 (ISSN-L)
- 0140-6736
- OpenAlex
- W1992307061
- Cited by
- 381
- References
- 19
- FWCI
- 10.02
- Type
- journal article
- Language
- en
- Open access
- closed
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- This page
- CoChat. (2026). Citation check: Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR). https://app.cochat.ai/papers/10.1016/0140-6736(91)90136-d
- The paper
- Zeviani, M., Gellera, C., Antozzi, C., Rimoldi, M., Morandi, L., Tiranti, V., DiDonato, S., & Villani, F. (1991). Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR). The Lancet. https://doi.org/10.1016/0140-6736(91)90136-d
Data sources
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.
