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Q24532123-43224B95-359D-4FCE-9F8F-E09E0CD23536
Q24532123-43224B95-359D-4FCE-9F8F-E09E0CD23536
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http://www.wikidata.org/entity/statement/Q24532123-43224B95-359D-4FCE-9F8F-E09E0CD23536
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation
P2860
Q24532123-43224B95-359D-4FCE-9F8F-E09E0CD23536
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24532123-43224B95-359D-4FCE-9F8F-E09E0CD23536
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wasDerivedFrom
97cbc3c5095fd246d9283e7bbe427a27b39bb8e5
P2860
Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome