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Q42291746-AE173B10-4EDD-4515-91DE-91C65D85F009
Q42291746-AE173B10-4EDD-4515-91DE-91C65D85F009
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-AE173B10-4EDD-4515-91DE-91C65D85F009
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.
P2860
Q42291746-AE173B10-4EDD-4515-91DE-91C65D85F009
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-AE173B10-4EDD-4515-91DE-91C65D85F009
rank
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type
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Statement
wasDerivedFrom
ec4207bc955d55300fb3cb5eee84a443b28ec621
P2860
Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders