A. Balfe

Peroxisomal bifunctional enzyme deficiency.

A. Moser, P. Watkins, R. Kelley, 1989, The Journal of clinical investigation.

Evaluation of serum transferrin receptor assay in a centralized iron screening service.

S. O'broin, B. Kelleher, C. Mc Mahon, 2005, Clinical and laboratory haematology.

Aberrant Subcellular Localization of Peroxisomal 3-Ketoacyl-CoA Thiolase in the Zellweger Syndrome and Rhizomelic Chondrodysplasia Punctata

P. Watkins, G. Hoefler, Winston W. Chen, 1990, Pediatric Research.

Study of peroxisomal proteins in patients with zellweger syndrome

H. Moser, J. Gärtner, W. Chen, 1990, Journal of Inherited Metabolic Disease.

Import of human bifunctional enzyme into peroxisomes of human hepatoma cells in vitro.

G. Hoefler, W. Chen, G. L. Chen, 1991, Biochemical and biophysical research communications.