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Publications by Ronald J.A. Wanders

Genetic Classification and Mutational Spectrum of More Than 600 Patients With a Zellweger Syndrome Spectrum Disorder

English

Inhibition of Hepatic Carnitine Palmitoyl-Transferase I (CPT IA) by Valproyl-CoA as a Possible Mechanism of Valproate-Induced Steatosis

Biochemical Pharmacology

English

Mutational Spectrum in the PEX7 Gene and Functional Analysis of Mutant Alleles in 78 Patients With Rhizomelic Chondrodysplasia Punctata Type 1

American Journal of Human Genetics

English

Genetic Basis of Peroxisome-Assembly Mutants of Humans, Chinese Hamster Ovary Cells, and Yeast: Identification of a New Complementation Group of Peroxisome-Biogenesis Disorders Apparently Lacking Peroxisomal-Membrane Ghosts

American Journal of Human Genetics

English

A PEX6-Defective Peroxisomal Biogenesis Disorder With Severe Phenotype in an Infant, Versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents

American Journal of Human Genetics

English

Mitochondrial Long Chain Fatty Acid Β-Oxidation in Man and Mouse

Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids

Molecular Biology

English