F.W. Verheijen

Update Persondata

• acid
• activity
• membrane
• mutations
• patients
• protein

Publications

(the most recent at the top)

Loss of nuclear activity of the FBXO7 protein in patients with parkinsonian-pyramidal syndrome (PARK15)

Mucopolysaccharidosis type IIIB may predominantly present with an attenuated clinical phenotype

Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome

Purification of the lysosomal sialic acid transporter. Functional characteristics of a monocarboxylate transporter

Lysosomal neuraminidase in human genetic diseases

Completed research projects

(the most recent research is at the top)
Researcher	Relation between clinical, biochemical and genetic heterogeneity in lysosomal storage diseases
Project leader	Hereditary defects in transport processes in the lysosomal membrane