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Q24681184-EB628610-1704-4D66-8A87-6398C523714A
Q24681184-EB628610-1704-4D66-8A87-6398C523714A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-EB628610-1704-4D66-8A87-6398C523714A
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-EB628610-1704-4D66-8A87-6398C523714A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-EB628610-1704-4D66-8A87-6398C523714A
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wasDerivedFrom
ca32dfdab5178724f8b98aa001f1190549e58a47
P2860
The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor