Inge Cuppen

Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein

The molecular basis of human retinal and vitreoretinal diseases

CLN3, the protein associated with batten disease: Structure, function and localization

Novel families of vacuolar amino acid transporters

Glycoproteomics

Congenital Disorders of Glycosylation from a Neurological Perspective

ALG11-CDG: Three novel mutations and further characterization of the phenotype

Tissue Expression and Subcellular Localization of CLN3, the Batten Disease Protein