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Q24645143-0826F5E3-CF57-4618-B6CA-4AED229BE8E7
Q24645143-0826F5E3-CF57-4618-B6CA-4AED229BE8E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24645143-0826F5E3-CF57-4618-B6CA-4AED229BE8E7
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
P2860
Q24645143-0826F5E3-CF57-4618-B6CA-4AED229BE8E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24645143-0826F5E3-CF57-4618-B6CA-4AED229BE8E7
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type
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wasDerivedFrom
e3c32c72cdb128c4c6f3c7b41447ea18adbe1203
P2860
Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders