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s10072-012-1129-3
s10072-012-1129-3
https://scigraph.springernature.com/pub.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.
P2888
Q46039775-B0C562D9-A441-4DCB-A262-02D6F2D5B861
P2888
s10072-012-1129-3
https://scigraph.springernature.com/pub.10.1007/s10072-012-1129-3