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eIF2B Modulators in Vanishing White Matter

eIF2B Modulators in Vanishing White Matter

Vanishing White Matter (VWM) disease is a rare and fatal leukodystrophy, caused by recessive mutations in the five genes encoding the protein complex eukaryotic translation initiation factor 2B (eIF2B). eIF2B plays a crucial role in initiating and regulating the...

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