Complex I deficiency and Leigh syndrome through the eyes of a clinician
Graphical Abstract 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
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| Principais autores: | , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Springer Nature
2020-10-01
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| Serija: | EMBO Molecular Medicine |
| Online dostop: | https://doi.org/10.15252/emmm.202013187 |
| Oznake: |
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