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Q38901362-60CBD5B4-567B-4F20-8877-036FF8B7715B
Q38901362-60CBD5B4-567B-4F20-8877-036FF8B7715B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38901362-60CBD5B4-567B-4F20-8877-036FF8B7715B
Mutant eIF2B leads to impaired mitochondrial oxidative phosphorylation in vanishing white matter disease.
P2860
Q38901362-60CBD5B4-567B-4F20-8877-036FF8B7715B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38901362-60CBD5B4-567B-4F20-8877-036FF8B7715B
rank
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type
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wasDerivedFrom
faed9aad56d6c8d4e9bad005e245dea54b1c72fd
P2860
EIF2B5 mutations compromise GFAP+ astrocyte generation in vanishing white matter leukodystrophy