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Q42291746-068F6771-BF69-459F-B4A4-86DB8DA7FBB2
Q42291746-068F6771-BF69-459F-B4A4-86DB8DA7FBB2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-068F6771-BF69-459F-B4A4-86DB8DA7FBB2
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders.
P2860
Q42291746-068F6771-BF69-459F-B4A4-86DB8DA7FBB2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42291746-068F6771-BF69-459F-B4A4-86DB8DA7FBB2
rank
NormalRank
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Statement
wasDerivedFrom
ec4207bc955d55300fb3cb5eee84a443b28ec621
P2860
A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotype.