Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.
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H. Waterham | R. Wanders | P. Barth | J. Epplen | C. Klein | G. Dodt | W. Kunau | C. Walter | J. Gootjes | P. Mooijer | H. Portsteffen
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H. Waterham | R. Wanders | P. Barth | J. Epplen | C. Klein | G. Dodt | W. Kunau | C. Walter | J. Gootjes | P. Mooijer | H. Portsteffen