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A case of vanishing white matter disease due to the c.260C > T(p.Ala87Val) EIF2B3 mutation
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RDF description of A case of vanishing white matter disease due to the c.260C > T(p.Ala87Val) EIF2B3 mutation - http://irises.unimi.it/resource/item/296932
rights: termsOfUse
date: 2026-08-03T13:32:47
publisher: A case of vanishing white matter disease due to the c.260C > T(p.Ala87Val) EIF2B3 mutation
type: Document