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- 7.9.1399 doi "10.1093/hmg/7.9.1399".
- 7.9.1399 isCitedBy PEX10.
- 7.9.1399 issue "9".
- 7.9.1399 journal "Hum. Mol. Genet.".
- 7.9.1399 pages "1399–405".
- 7.9.1399 pmid "9700193".
- 7.9.1399 title "Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.".
- 7.9.1399 vauthors "Okumoto K, Itoh R, Shimozawa N, etal".
- 7.9.1399 volume "7".
- 7.9.1399 year "1998".