PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p
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T. Tsukamoto | N. Shimozawa | K. Okumoto | A. Kawai | S. Tamura | T. Osumi | H. Moser | R. Wanders | Yasuyuki Suzuki | Naomi Kondo | Y. Fujiki | N. Kondo