Peter Mayerhofer

Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G

Ania C. Muntau, Peter Mayerhofer, Barbara C. Paton et al. · The American Journal of Human Genetics · 2000 · 109 citations

Life Sciences, Genetics, Molecular Genetics +13

Mutations in the Proenteropeptidase Gene Are the Molecular Cause of Congenital Enteropeptidase Deficiency

Andreas Holzinger, Esther M. Maier, Cornelius Bück et al. · The American Journal of Human Genetics · 2002 · 97 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity ofMCCA andMCCB mutations and impact on risk assessment

Sonja C. Stadler, Roman Polanetz, Esther M. Maier et al. · Human Mutation · 2006 · 89 citations

Medicine, Genetics, Pediatrics +16

Structure of the Inhibited State of the Sec Translocon

S. Gerard, Belinda S. Hall, A. Zaki et al. · Molecular Cell · 2020 · 72 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +13

Human Adrenoleukodystrophy Protein and Related Peroxisomal ABC Transporters Interact with the Peroxisomal Assembly Protein PEX19p

Christian Johannes Gloeckner, Peter Mayerhofer, Pablo Landgraf et al. · Biochemical and Biophysical Research Communications · 2000 · 57 citations

Life Sciences, Molecular Biology, Molecular Genetics +12