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Q46039775-A3532AB4-C8E8-45E8-B1B8-E1C91EC47B57
Q46039775-A3532AB4-C8E8-45E8-B1B8-E1C91EC47B57
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46039775-A3532AB4-C8E8-45E8-B1B8-E1C91EC47B57
Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course.
P31
Q46039775-A3532AB4-C8E8-45E8-B1B8-E1C91EC47B57
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46039775-A3532AB4-C8E8-45E8-B1B8-E1C91EC47B57
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
d851d705f4f373e1f70d98ffd2e133cf168d402c
P31
scholarly article