Mitochondrial involvement in a Bosch-Boonstra-Schaaf optic atrophy syndrome patient with a novel de novo NR2F1 gene mutation

  1. Martín-Hernández, E.
  2. Rodríguez-García, M.E.
  3. Chen, C.-A.
  4. Cotrina-Vinagre, F.J.
  5. Carnicero-Rodríguez, P.
  6. Bellusci, M.
  7. Schaaf, C.P.
  8. Martínez-Azorín, F.
Journal:
Journal of Human Genetics

ISSN: 1435-232X 1434-5161

Year of publication: 2018

Volume: 63

Issue: 4

Pages: 525-528

Type: Article

DOI: 10.1038/S10038-017-0398-3 GOOGLE SCHOLAR

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