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

Document Type

Article

Author

Bertacchi, M.; Serra, L.; Studer, M.; Gruart, A.; Delgado-García, J.M.; Kaimakis, P.; Bovolenta, P.; Allet, C.; Giacobini, P.

Source

In: EMBO Molecular Medicine. (EMBO Molecular Medicine, 2019, 11(8))

Subject

Language

English

ISSN

17574684
17574676

Online Access

Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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