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Q34921167-B73725EE-3F3D-41CF-976D-576F6F2518C2
Q34921167-B73725EE-3F3D-41CF-976D-576F6F2518C2
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Statement
http://www.wikidata.org/entity/statement/Q34921167-B73725EE-3F3D-41CF-976D-576F6F2518C2
Rational diagnostic strategy for Zellweger syndrome spectrum patients
P2860
Q34921167-B73725EE-3F3D-41CF-976D-576F6F2518C2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34921167-B73725EE-3F3D-41CF-976D-576F6F2518C2
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bca8049e49ca8f1d2b6db8c7908104a6884383ae
P2860
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation