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Q24681184-36802ADD-3399-45D1-81CC-6A547A5087F9
Q24681184-36802ADD-3399-45D1-81CC-6A547A5087F9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-36802ADD-3399-45D1-81CC-6A547A5087F9
Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease
P2860
Q24681184-36802ADD-3399-45D1-81CC-6A547A5087F9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-36802ADD-3399-45D1-81CC-6A547A5087F9
rank
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wasDerivedFrom
ca32dfdab5178724f8b98aa001f1190549e58a47
P2860
Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders