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 · Full text

Molecular Physiology, Mendelian Disorder, Complementation Group G +7

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 · 94 citations · Full text

Developmental Biology, Genetic Disorder, Medicine +11

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

Structure of the Inhibited State of the Sec Translocon

S. Gerard, Belinda S. Hall, A. Zaki et al. · Molecular Cell · 2020 · 71 citations · Full text

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 · 56 citations

Protein Function, Molecular Physiology, Biochemistry +5