Author:
Alexander D. R.,Deeb M.,Jackson M.,Marsh J.,Fensom A. H.
Subject
Genetics (clinical),Genetics
Reference3 articles.
1. Alexander, D. R., Deeb, M. and Talj, F. Heterozygosity of phosphodiester glycosidase deficiency: a novel human mutation of lysosomal enzyme processing.Hum. Genet. (1986) in press
2. Alexander, D. R., Dudin, G., Talj, F., Bitar, F., Deeb, M., Khudr, A., Abboud, M. and Der Kaloustian, V. M. Five related Lebanese individuals with high plasma lysosomal hydrolases: a new defect in mannose-6-phosphate receptor recognition?Am. J. Hum. Genet. 36 (1984) 1004–1014
3. Den Tandt, W. R. Affinity chromatography of lysosomal enzymes in plasma, urine and fibroblasts of patients with mucolipidosis II and III.Clin. Chim. Acta 102 (1980) 199–205