Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.
暂无分享，去创建一个
R. Wanders | A. Imamura | Y. Suzuki | N. Shimozawa | K. Okumoto | T. Osumi | Y. Fujiki | N. Kondo | P. Barth | T. Tsukamoto | K. Tateishi | T. Orii | Z. Zhang