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Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course
Luisa Sambati, Raffaele Agati, Antonella Bacci, Silvia Bianchi, Sabina CapellariVolume:
34
Language:
english
DOI:
10.1007/s10072-012-1129-3
Date:
July, 2013
File:
PDF, 306 KB
english, 2013