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Multimodal single-cell analysis of nonrandom heteroplasmy distribution in human retinal mitochondrial disease
Variants within the high copy number mitochondrial genome (mtDNA) can disrupt organelle function and lead to severe multisystem disease. The wide range of manifestations observed in patients with mitochondrial disease results from varying fractions of abnormal mtDNA molecules in different cells and...
Autores principales: | Mullin, Nathaniel K., Voigt, Andrew P., Flamme-Wiese, Miles J., Liu, Xiuying, Riker, Megan J., Varzavand, Katayoun, Stone, Edwin M., Tucker, Budd A., Mullins, Robert F. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10443808/ https://www.ncbi.nlm.nih.gov/pubmed/37289546 http://dx.doi.org/10.1172/jci.insight.165937 |
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