[Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy].
- DOI
- 10.1016/j.medcli.2015.10.015
- Published
- 2016 Feb 19
- Container
- Medicina clinica
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.medcli.2015.10.015,
title = {[Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy].},
author = {Carrasco Salas P and Palma Milla C and López Montiel J and Benito C and Franco Freire S and López Siles J},
year = {2016},
journal = {Medicina clinica},
doi = {10.1016/j.medcli.2015.10.015},
url = {https://doi.org/10.1016/j.medcli.2015.10.015}
}RIS
TY - JOUR TI - [Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy]. AU - Carrasco Salas P AU - Palma Milla C AU - López Montiel J AU - Benito C AU - Franco Freire S AU - López Siles J PY - 2016 JO - Medicina clinica DO - 10.1016/j.medcli.2015.10.015 UR - https://doi.org/10.1016/j.medcli.2015.10.015 ER -
APA
P, C. S., C, P. M., J, L. M., C, B., S, F. F., & J, L. S. (2016). [Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy].. Medicina clinica. https://doi.org/10.1016/j.medcli.2015.10.015
Source records
- pubmed · retrieved 2026-09-25T09:18:30.432Z