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Q22008461-C5F9C83B-A6C2-43CB-B87C-062000429243
Q22008461-C5F9C83B-A6C2-43CB-B87C-062000429243
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Statement
http://www.wikidata.org/entity/statement/Q22008461-C5F9C83B-A6C2-43CB-B87C-062000429243
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
P2860
Q22008461-C5F9C83B-A6C2-43CB-B87C-062000429243
BestRank
Statement
http://www.wikidata.org/entity/statement/Q22008461-C5F9C83B-A6C2-43CB-B87C-062000429243
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wasDerivedFrom
f46b321aeb85daea8be577f8a27b874ce47fde12
P2860
Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders