Shimozawa, Nobuyuki: "Peroxisome biogenesis disorders : identification of a new complementation group distinct from peroxisome deficient CHO mutants and not complemented by human PEX13" Biochemical and Biophysical Research Communications. (印刷中).
Shimozawa, Nobuyuki: "Peroxisome biogenesis disorders : identification of a new complementation group distinct from peroxisome deficient CHO mutants and not complemented by human PEX13" Biochemical and Biophysical Research Communications. (印刷中).
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Shimozawa, Nobuyuki:“过氧化物酶体生物发生障碍:鉴定出与过氧化物酶体缺陷的 CHO 突变体不同且不被人类 PEX13 补充的新互补组”《生物化学和生物物理研究通讯》(正在出版)。
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