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Q24681184-D805FC57-99F7-4396-A614-2F3E4479406B
Q24681184-D805FC57-99F7-4396-A614-2F3E4479406B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-D805FC57-99F7-4396-A614-2F3E4479406B
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-D805FC57-99F7-4396-A614-2F3E4479406B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-D805FC57-99F7-4396-A614-2F3E4479406B
rank
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wasDerivedFrom
ca32dfdab5178724f8b98aa001f1190549e58a47
P2860
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders