Mosaicism for sulfoiduronate sulfatase deficiency in carriers of Hunter's syndrome
- 1 April 1976
- journal article
- specialia
- Published by Springer Nature in Cellular and Molecular Life Sciences
- Vol. 32 (4) , 459-460
- https://doi.org/10.1007/bf01920795
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- New method for mapping genes in human chromosomesNature, 1975
- An assay for iduronate sulfatase (hunter corrective factor)Carbohydrate Research, 1974
- Aspects ultrastructuraux et signification biochimique des granulations métachromatiques et autres inclusions dans les fibroblastes en culture provenant de lipidoses et de mucopolysaccharidosesJournal of the Neurological Sciences, 1973
- Human Phosphoglycerate Kinase and Inactivation of the X ChromosomeScience, 1972
- Genetic Inactivation of the α-Galactosidase Locus in Carriers of Fabry's DiseaseScience, 1970
- CULTIVATED AMNIOTIC-FLUID CELLS AND FIBROBLASTS DERIVED FROM FAMILIES WITH CYSTIC FIBROSISThe Lancet, 1969
- X-Linked Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency: Heterozygote Has Two Clonal PopulationsScience, 1968
- HURLER'S SYNDROMEThe Journal of Experimental Medicine, 1966
- Gene Action in the X-chromosome of the Mouse (Mus musculus L.)Nature, 1961
- [73] Spectrophotometric and turbidimetric methods for measuring proteinsPublished by Elsevier ,1957