Peroxisome Biogenesis Disorders: Identification of a New Complementation Group Distinct from Peroxisome-Deficient CHO Mutants and Not Complemented by Human PEX 13

Author: Shimozawa N.   Suzuki Y.   Zhang Z.   Imamura A.   Tsukamoto T.   Osumi T.   Tateishi K.   Okumoto K.   Fujiki Y.   Orii T.   Barth P.G.   Wanders R.J.A.   Kondo N.  

Publisher: Elsevier

ISSN: 0006-291X

Source: Biochemical and Biophysical Research Communications, Vol.243, Iss.2, 1998-02, pp. : 368-371

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content