Identification and characterization of new variants in FOXRED1 gene expands the clinical spectrum associated with mitochondrial complex I deficiency
- Barbosa-Gouveia, S.
- González-Vioque, E.
- Borges, F.
- Gutiérrez-Solana, L.
- Wintjes, L.
- Kappen, A.
- Van Den Heuvel, L.
- Leis, R.
- Rodenburg, R.
- Couce, M.L.
Journal:
Journal of Clinical Medicine
ISSN: 2077-0383
Year of publication: 2019
Volume: 8
Issue: 8
Type: Article