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
Сохранить в:
| Главные авторы: | , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Springer Nature
2020-10-01
|
| Серии: | EMBO Molecular Medicine |
| Online-ссылка: | https://doi.org/10.15252/emmm.202013187 |
| Метки: |
Нет меток, Требуется 1-ая метка записи!
|