Mouse Nr2f1 haploinsufficiency unveils new pathological mechanisms of a human optic atrophy syndrome

  1. Bertacchi, M.
  2. Gruart, A.
  3. Kaimakis, P.
  4. Allet, C.
  5. Serra, L.
  6. Giacobini, P.
  7. Delgado-García, J.M.
  8. Bovolenta, P.
  9. Studer, M.
Revue:
EMBO Molecular Medicine

ISSN: 1757-4684,  1757-4676

Année de publication: 2019

Volumen: 11

Número: 8

Type: Article

DOI: 10.15252/EMMM.201910291 GOOGLE SCHOLAR lock_openAccès ouvert editor
La source de données: Scopus