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Q24681184-E95F6E0E-D6C5-4598-8095-501AB77E64F1
Q24681184-E95F6E0E-D6C5-4598-8095-501AB77E64F1
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http://www.wikidata.org/entity/statement/Q24681184-E95F6E0E-D6C5-4598-8095-501AB77E64F1
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-E95F6E0E-D6C5-4598-8095-501AB77E64F1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24681184-E95F6E0E-D6C5-4598-8095-501AB77E64F1
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wasDerivedFrom
ca32dfdab5178724f8b98aa001f1190549e58a47
P2860
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders