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Q24645143-BE81CCFA-F369-4561-9ABD-4CAA531D8BA5
Q24645143-BE81CCFA-F369-4561-9ABD-4CAA531D8BA5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24645143-BE81CCFA-F369-4561-9ABD-4CAA531D8BA5
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
P2860
Q24645143-BE81CCFA-F369-4561-9ABD-4CAA531D8BA5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24645143-BE81CCFA-F369-4561-9ABD-4CAA531D8BA5
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wasDerivedFrom
e3c32c72cdb128c4c6f3c7b41447ea18adbe1203
P2860
The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor