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Mutant eIF2B leads to impaired mitochondrial oxidative phosphorylation in vanishing white matter disease.
J Neurochem. 2017 Jun;141(5):694-707. doi: 10.1111/jnc.14024. Epub 2017 Apr 16.
J Neurochem. 2017.
PMID: 28306143
Free article.
Proteomics-level analysis of myelin formation and regeneration in a mouse model for Vanishing White Matter disease.
Gat-Viks I, Geiger T, Barbi M, Raini G, Elroy-Stein O.
Gat-Viks I, et al. Among authors: raini g.
J Neurochem. 2015 Aug;134(3):513-26. doi: 10.1111/jnc.13142. Epub 2015 May 14.
J Neurochem. 2015.
PMID: 25920008
Free PMC article.
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A mouse model for eukaryotic translation initiation factor 2B-leucodystrophy reveals abnormal development of brain white matter.
Geva M, Cabilly Y, Assaf Y, Mindroul N, Marom L, Raini G, Pinchasi D, Elroy-Stein O.
Geva M, et al. Among authors: raini g.
Brain. 2010 Aug;133(Pt 8):2448-61. doi: 10.1093/brain/awq180.
Brain. 2010.
PMID: 20826436
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