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[文献書誌] Mitsuo Masuno: "Assignment of the human peroxisome assembly factor-1 gene(PXMP3) responsible for Zellweger syndrome to chromosome 8g21.1 by fluorescence in situ hybridization" Geomics. (in press). (1994)
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[文献書誌] Yasuyuki Suzuki: "Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with delectable enzyme protein:Identification by means of complementation analysis" Am.J.Hum.Genet.54. 36-43 (1994)
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[文献書誌] Yasuyuki suzuki: "Perdxissanrl 3-ketoacyl-CoA thiolose is partially processed infibroblasts from patients with Rhizomelic chondrodysplasia punctata" J.Inher.Metnb.Dis.16. 868-871 (1993)
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[文献書誌] Nobuyuki Shimozawa: "Standardization of complementation prouping ofperoxisome-deficient disovclers and the second Zellweger patient with PAF-1 defect" Am.J.Hum.Genet.52. 843-844 (1993)
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[文献書誌] Nobuyuki Shimozawa: "Prenatal dicgnosis of Zellweger synchcme using DNA analysis" Prenatal Diagnosis. 13. 149- (1993)
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[文献書誌] 下沢伸行: "ペルオキシソーム欠損症 神経疾患の分子医学 辻省次(編)" 羊土社, 148 (1993)