Scheie and Hurler Syndromes: Apparent Identity of the Biochemical Defect
- 3 July 1970
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 169 (3940), 72-74
- https://doi.org/10.1126/science.169.3940.72
Abstract
Fibroblasts cultured from the skin of Scheie and Hurler patients are deficient in the same specific factor required for normal mucopolysaccharide metabolism.Keywords
This publication has 6 references indexed in Scilit:
- Inborn Errors of Mucopolysaccharide MetabolismScience, 1970
- Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresisBiochemical and Biophysical Research Communications, 1970
- Classification of the mucopolysaccharidoses based on the pattern of mucopolysacchariduriaAmerican Journal Of Medicine, 1969
- Hurler and Hunter Syndromes: Mutual Correction of the Defect in Cultured FibroblastsScience, 1968
- A method for separation of chondroitin sulfate B from isomers A and C by paper electrophoresis with zinc sulphate or zinc acetate solution as electrolyte mediumBiochimica et Biophysica Acta (BBA) - General Subjects, 1967
- A Newly Recognized Forme Fruste of Hurler's Disease (Gargoylism)* *From the Departments of Ophthalmology, Dermatology, and Pediatrics, Hospital of the University of Pennsylvania, Children's Hospital of Philadelphia, and University of Pennsylvania Medical School.American Journal of Ophthalmology, 1962