Mouse Nr2f1 haploinsufficiency unveils new pathological mechanisms of a human optic atrophy syndrome
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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Mouse Nr2f1 haploinsufficiency unveils new pathological mechanisms of a human optic atrophy syndrome ; volume:11 ; number:8 ; year:2019 ; extent:18
EMBO molecular medicine / European Molecular Biology Organization ; 11, Heft 8 (2019) (gesamt 18)
- Urheber
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Bertacchi, Michele
Gruart, Agnès
Kaimakis, Polynikis
Allet, Cécile
Serra, Linda
Giacobini, Paolo
Delgado‐García, José M.
Bovolenta, Paola
Studer, Michèle
- DOI
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10.15252/emmm.201910291
- URN
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urn:nbn:de:101:1-2022080307154612344669
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:21 MESZ
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Beteiligte
- Bertacchi, Michele
- Gruart, Agnès
- Kaimakis, Polynikis
- Allet, Cécile
- Serra, Linda
- Giacobini, Paolo
- Delgado‐García, José M.
- Bovolenta, Paola
- Studer, Michèle
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