Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency

  1. Morán, M.
  2. Marín-Buera, L.
  3. Carmen Gil-Borlado, M.
  4. Rivera, H.
  5. Blázquez, A.
  6. Seneca, S.
  7. Vázquez-López, M.
  8. Arenas, J.
  9. Martín, M.A.
  10. Ugalde, C.
Journal:
Human Mutation

ISSN: 1059-7794 1098-1004

Year of publication: 2010

Volume: 31

Issue: 8

Pages: 930-941

Type: Article

DOI: 10.1002/HUMU.21294 GOOGLE SCHOLAR

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