van Faassen, H.

Biochemical studies on the enzymatic deficiencies in hereditary tyrosinemia

Berger, R., van Faassen, H., & Smith, G. P. A. (1983) · Clinica Chimica Acta

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 45

Type I Tyrosinemia: Lack of Immunologically Detectable Fumarylacetoacetase Enzyme Protein in Tissues and Cell Extracts

Berger, R., Van Faassen, H., Taanman, J. W., De Vries, H., & Agsteribbe, E. (1987) · Pediatric Research

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 37

Hereditary Tyrosinemia Type I: Lack of Correlation between Clinical Findings and Amount of Immunoreactive Fumarylacetoacetase Protein

Kvittingen, E. A., Rootwelt, H., van Dam, T., van Faassen, H., & Berger, R. (1992) · Pediatric Research

Metabolism and Genetic DisordersAmino Acid Enzymes and Metabolism

Cited by 21