Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency
- DOI
- 10.1002/humu.21294
- Published
- 2010-06-22
- Container
- Human Mutation
- Publisher
- Hindawi Limited
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/humu.21294,
title = {Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency},
author = {María Morán and Lorena Marín-Buera and M. Carmen Gil-Borlado and Henry Rivera and Alberto Blázquez and Sara Seneca and María Vázquez-López and Joaquín Arenas and Miguel A. Martín and Cristina Ugalde},
year = {2010},
journal = {Human Mutation},
doi = {10.1002/humu.21294},
url = {https://doi.org/10.1002/humu.21294}
}RIS
TY - JOUR TI - Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency AU - María Morán AU - Lorena Marín-Buera AU - M. Carmen Gil-Borlado AU - Henry Rivera AU - Alberto Blázquez AU - Sara Seneca AU - María Vázquez-López AU - Joaquín Arenas AU - Miguel A. Martín AU - Cristina Ugalde PY - 2010 JO - Human Mutation DO - 10.1002/humu.21294 UR - https://doi.org/10.1002/humu.21294 ER -
APA
Morán, M., Marín-Buera, L., Gil-Borlado, M. C., Rivera, H., Blázquez, A., Seneca, S., Vázquez-López, M., Arenas, J., Martín, M. A., & Ugalde, C. (2010). Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency. Human Mutation. https://doi.org/10.1002/humu.21294
Source records
- crossref · retrieved 2026-11-05T05:46:35.850Z