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1 records found for search term Eif2b4
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RGD IDTitleCitationAbstractPubMedPub Date
11343692Adult-onset vanishing white matter disease with novel missense mutations in a subunit of translational regulator, EIF2B4.Kanbayashi T, etal., Clin Genet. 2015 Oct;88(4):401-3. doi: 10.1111/cge.12554. Epub 2015 Jan 20.256000652015-07-01