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Q24681184-7C87EAF2-1677-42F7-9827-DE64202E21A7
Q24681184-7C87EAF2-1677-42F7-9827-DE64202E21A7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-7C87EAF2-1677-42F7-9827-DE64202E21A7
Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease
P2860
Q24681184-7C87EAF2-1677-42F7-9827-DE64202E21A7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-7C87EAF2-1677-42F7-9827-DE64202E21A7
rank
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wasDerivedFrom
ca32dfdab5178724f8b98aa001f1190549e58a47
P2860
Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a cycling receptor