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Mutant eIF2B leads to impaired mitochondrial oxidative phosphorylation in vanishing white matter disease
Raini, Gali, Sharet, Reut, Herrero, Melisa, Atzmon, Andrea, Shenoy, Anjana, Geiger, Tamar, Elroy-Stein, OrnaLanguage:
english
Journal:
Journal of Neurochemistry
DOI:
10.1111/jnc.14024
Date:
April, 2017
File:
PDF, 791 KB
english, 2017