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Current and Emerging Clinical Treatment in Mitochondrial Disease
Primary mitochondrial disease (PMD) is a group of complex genetic disorders that arise due to pathogenic variants in nuclear or mitochondrial genomes. Although PMD is one of the most prevalent inborn errors of metabolism, it often exhibits marked phenotypic variation and can therefore be difficult t...
Autores principales: | Tinker, Rory J., Lim, Albert Z., Stefanetti, Renae J., McFarland, Robert |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919238/ https://www.ncbi.nlm.nih.gov/pubmed/33646563 http://dx.doi.org/10.1007/s40291-020-00510-6 |
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