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Q46039775-59F239D5-99CF-4622-B54A-2DB7C9175333
Q46039775-59F239D5-99CF-4622-B54A-2DB7C9175333
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46039775-59F239D5-99CF-4622-B54A-2DB7C9175333
Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course.
P2860
Q46039775-59F239D5-99CF-4622-B54A-2DB7C9175333
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46039775-59F239D5-99CF-4622-B54A-2DB7C9175333
rank
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wasDerivedFrom
e6db9944c429c4f9ee8f177cd9af70c10bdcd1ad
P2860
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter