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Q42291746-E899925B-4477-4699-88F5-D811C4749202
Q42291746-E899925B-4477-4699-88F5-D811C4749202
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-E899925B-4477-4699-88F5-D811C4749202
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.
P2860
Q42291746-E899925B-4477-4699-88F5-D811C4749202
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-E899925B-4477-4699-88F5-D811C4749202
rank
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type
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Statement
wasDerivedFrom
ec4207bc955d55300fb3cb5eee84a443b28ec621
P2860
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders