Diaphragmatic Mitochondrial Myopathy in a Patient-Derived Mouse Model of Barth Syndrome.
- DOI
- 10.3390/jdb14030040
- Published
- 2026 Sep 3
- Container
- Journal of developmental biology
- Publisher
- Not recorded
- Open access
- unknown
Credibility signals
limited evidence Score 43/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.3390/jdb14030040,
title = {Diaphragmatic Mitochondrial Myopathy in a Patient-Derived Mouse Model of Barth Syndrome.},
author = {Tentler K and Snider PL and Matias C and Brault JJ and Conway SJ},
year = {2026},
journal = {Journal of developmental biology},
doi = {10.3390/jdb14030040},
url = {https://doi.org/10.3390/jdb14030040}
}RIS
TY - JOUR TI - Diaphragmatic Mitochondrial Myopathy in a Patient-Derived Mouse Model of Barth Syndrome. AU - Tentler K AU - Snider PL AU - Matias C AU - Brault JJ AU - Conway SJ PY - 2026 JO - Journal of developmental biology DO - 10.3390/jdb14030040 UR - https://doi.org/10.3390/jdb14030040 ER -
APA
K, T., PL, S., C, M., JJ, B., & SJ, C. (2026). Diaphragmatic Mitochondrial Myopathy in a Patient-Derived Mouse Model of Barth Syndrome.. Journal of developmental biology. https://doi.org/10.3390/jdb14030040
Source records
- pubmed · retrieved 2026-09-25T08:27:44.225Z