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S10072-012-1129-3
S10072-012-1129-3
http://dx.doi.org/10.1007/S10072-012-1129-3
Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course.
P356
Q46039775-F5824B18-3EA7-4B85-A1B4-A05BC816F4B3
P356
S10072-012-1129-3
http://dx.doi.org/10.1007/S10072-012-1129-3