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Q24532123-8073F2B9-8321-4E4E-A785-F9C16B87F2AF
Q24532123-8073F2B9-8321-4E4E-A785-F9C16B87F2AF
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Statement
http://www.wikidata.org/entity/statement/Q24532123-8073F2B9-8321-4E4E-A785-F9C16B87F2AF
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation
P2860
Q24532123-8073F2B9-8321-4E4E-A785-F9C16B87F2AF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24532123-8073F2B9-8321-4E4E-A785-F9C16B87F2AF
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wasDerivedFrom
97cbc3c5095fd246d9283e7bbe427a27b39bb8e5
P2860
Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells.