Identification and characterization of new variants in FOXRED1 gene expands the clinical spectrum associated with mitochondrial complex I deficiency

  1. Barbosa-Gouveia, S.
  2. González-Vioque, E.
  3. Borges, F.
  4. Gutiérrez-Solana, L.
  5. Wintjes, L.
  6. Kappen, A.
  7. Van Den Heuvel, L.
  8. Leis, R.
  9. Rodenburg, R.
  10. Couce, M.L.
Revista:
Journal of Clinical Medicine

ISSN: 2077-0383

Ano de publicación: 2019

Volume: 8

Número: 8

Tipo: Artigo

DOI: 10.3390/JCM8081262 GOOGLE SCHOLAR lock_openAcceso aberto editor
Fonte de datos: Scopus