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Q22008461-2E601502-9C09-463A-8218-BE6571BA680E
Q22008461-2E601502-9C09-463A-8218-BE6571BA680E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008461-2E601502-9C09-463A-8218-BE6571BA680E
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
P2860
Q22008461-2E601502-9C09-463A-8218-BE6571BA680E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008461-2E601502-9C09-463A-8218-BE6571BA680E
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wasDerivedFrom
f46b321aeb85daea8be577f8a27b874ce47fde12
P2860
The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor