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Complex I deficiency and Leigh syndrome through the eyes of a clinician
K. Õunap and K. Reinson discuss the biochemical and functional characterization of the NDUFC2 pathogenic variants identified in children with Leigh syndrome by R. Taylor and colleagues, in this issue of EMBO Molecular Medicine [Image: see text]
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645367/ https://www.ncbi.nlm.nih.gov/pubmed/33124751 http://dx.doi.org/10.15252/emmm.202013187 |