Authors: Holzinger, A Maier, EM Buck, C Mayerhofer, PU Kappler, M Haworth, JC Moroz, SP Hadorn, HB Sadler, JE Roscher, AA

Citation: A. Holzinger et al., Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency, AM J HU GEN, 70(1), 2002, pp. 20-25

Authors: Holzinger, A Roschinger, W Lagler, F Mayerhofer, PU Lichtner, P Kattenfeld, T Thuy, L Nyhan, WL Koch, HG Muntau, AC Roscher, AA

Citation: A. Holzinger et al., Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency, HUM MOL GEN, 10(12), 2001, pp. 1299-1306

Authors: Muntau, AC Mayerhofer, PU Albet, S Schmid, TE Bugaut, M Roscher, AA Kammerer, S

Citation: Ac. Muntau et al., Genomic organization, expression analysis, and chromosomal localization ofthe mouse PEX3 gene encoding a peroxisomal assembly protein, BIOL CHEM, 381(4), 2000, pp. 337-342

Authors: Gloeckner, CJ Mayerhofer, PU Landgraf, P Muntau, AC Holzinger, A Gerber, JK Kammerer, S Adamski, J Roscher, AA

Citation: Cj. Gloeckner et al., Human adrenoleukodystrophy protein and related peroxisomal ABC transporters interact with the peroxisomal assembly protein PEX19p, BIOC BIOP R, 271(1), 2000, pp. 144-150

Authors: Muntau, AC Holzinger, A Mayerhofer, PU Gartner, J Roscher, AA Kammerer, S

Citation: Ac. Muntau et al., The human PEX3 gene encoding a peroxisomal assembly protein: Genomic organization, positional mapping, and mutation analysis in candidate phenotypes, BIOC BIOP R, 268(3), 2000, pp. 704-710

Authors: Muntau, AC Mayerhofer, PU Paton, BC Kammerer, S Roscher, AA

Citation: Ac. Muntau et al., Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G, AM J HU GEN, 67(4), 2000, pp. 967-975