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Mitochondrial Disease: Advances in clinical diagnosis, management, therapeutic development, and preventative strategies
PURPOSE OF REVIEW: Primary mitochondrial disease encompasses an impressive range of inherited energy deficiency disorders having highly variable molecular etiologies as well as clinical onset, severity, progression, and response to therapies of multi-system manifestations. Significant progress has b...
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| Publicado no: | Curr Genet Med Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6208355/ https://ncbi.nlm.nih.gov/pubmed/30393588 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40142-018-0138-9 |
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