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Q24290144-9E77CBF8-D4A7-43E2-B9E5-8C932BF08B16
Q24290144-9E77CBF8-D4A7-43E2-B9E5-8C932BF08B16
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http://www.wikidata.org/entity/statement/Q24290144-9E77CBF8-D4A7-43E2-B9E5-8C932BF08B16
Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G
P2860
Q24290144-9E77CBF8-D4A7-43E2-B9E5-8C932BF08B16
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24290144-9E77CBF8-D4A7-43E2-B9E5-8C932BF08B16
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wasDerivedFrom
d36b63eefaf83baae7e130f36dc7c8de1f120a4b
P2860
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly