Two Splice Variants of Human PEX19 Exhibit Distinct Functions in Peroxisomal Assembly von Mayerhofer, Peter U., Kattenfeld, Tanja, Roscher, Adelbert A., Muntau, Ania C.

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Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency von HOLZINGER, Andreas, RÖSCHINGER, Wulf, ROSCHER, Adelbert A, LAGLER, Florian, MAYERHOFER, Peter U, LICHTNER, Peter, KATTENFELD, Tanja, LE PHUC THUY, NYHAN, William L, KOCH, Hans G, MUNTAU, Ania C

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