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Q24603771-689F4123-1F02-4ECC-94A7-0BB9642F91AD
Q24603771-689F4123-1F02-4ECC-94A7-0BB9642F91AD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24603771-689F4123-1F02-4ECC-94A7-0BB9642F91AD
A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox
P2860
Q24603771-689F4123-1F02-4ECC-94A7-0BB9642F91AD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24603771-689F4123-1F02-4ECC-94A7-0BB9642F91AD
rank
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type
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Statement
wasDerivedFrom
72040f019f28e141dec4302999afda50a4e09275
P2860
Origin of mutations in two families with X-linked chronic granulomatous disease.