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...

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Detalles Bibliográficos
Autores principales: Tinker, Rory J., Lim, Albert Z., Stefanetti, Renae J., McFarland, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Review Article
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

Internet

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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