Aspartylglucosaminuria: Deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parents
- 1 May 1973
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 4 (3) , 297-300
- https://doi.org/10.1111/j.1399-0004.1973.tb01161.x
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Aspartylglucosaminuria II: biochemical studies on brain, liver, kidney and spleenActa Neuropathologica, 1972
- Aspartylglucosaminuria I: fine structural studies on liver, kidney and brainActa Neuropathologica, 1972
- Enzymatic cleavage of 2-acetamido-1-(β'-l-aspartamido)-1,2-dideoxy-β-d-glucose by human plasma and seminal fluid. Failure to detect the heterozygous state for aspartylgly-cosaminuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- ASPARTYLGLYCOSAMINURIAThe Lancet, 1968
- PREVALENCE OF PHENYLKETONURIA AND SOME OTHER METABOLIC DISORDERS AMONG MENTALLY RETARDED PATIENTS IN FINLANDActa Neurologica Scandinavica, 1967
- Enzymatic cleavage of glycopeptidesBiochemical and Biophysical Research Communications, 1966
- The assay of arylsulphatases A and B in human urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1959
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951