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377004
377004
http://dx.doi.org/10.1086/377004
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation
P356
Q24532123-893AC301-3C2B-4E10-B484-95FFAF8D10EA
P356
377004
http://dx.doi.org/10.1086/377004