Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course

Overview of attention for article published in Neurological Sciences, June 2012

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Patient diagnosed @ 18mnths old with Vanishing white matter + is now 37!!!!!!!!! http://t.co/x8MW3vRp http://t.co/x8MW3vRp

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