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[文献書誌] Imamura A, Suzuki Y, et al: "Temperature sensitive phenotypes of peroxisome assembly processes represent the milder forms of human peroxisome biogenesis disorders." Am J Hum Genet. 62. 1539-1543 (1998)
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[文献書誌] Honsho M, Suzuki Y, et al: "Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D." Am J Hum Genet. 63. 1622-1630 (1998)
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[文献書誌] Shimozawa N, Suzuki Y, et al: "Genetic basis of peroxisome assembly mutants of humans, CHO cells and yeast" Am J Hum Genet. 63. 1898-1903 (1998)
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[文献書誌] Imamura A, Suzuki Y, et al: "Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders in the highest-incidence group." Hum Mol Genet. 7. 2089-2094 (1998)
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[文献書誌] Grunsven EGv, Suzuki Y, et al: "Peroxisomal bifunctional protein deficiency revisited : resolution of its true enzymatic and molecular basis." Am J Hum Genet. (in press). (1999)
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[文献書誌] Suzuki Y, Zhang Z, et al: "Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency." J Human Genet. (in press). (1999)