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Q46039775-FA65446A-BF22-4AAD-972F-C84D1F49D080
Q46039775-FA65446A-BF22-4AAD-972F-C84D1F49D080
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46039775-FA65446A-BF22-4AAD-972F-C84D1F49D080
Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course.
P698
Q46039775-FA65446A-BF22-4AAD-972F-C84D1F49D080
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46039775-FA65446A-BF22-4AAD-972F-C84D1F49D080
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d851d705f4f373e1f70d98ffd2e133cf168d402c
P698
22729508
http://www.w3.org/2001/XMLSchema#string