Genetic aspects of mucopolysaccharidoses with special reference to heterozygous carriers
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Published:1975
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Volume:
Page:147-160
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ISSN:
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Container-title:Inborn Errors of Skin, Hair and Connective Tissue
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language:
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Publisher
Springer Netherlands
Reference33 articles.
1. Bach, G., Friedman, R., Weissmann, B. and Neufeld, E. F. (1972) The defect in the Hurler andScheie syndromes: deficiency of Liduronidase. Proceedings of the National Academy of Sciences of the U.S.A., 69, 2048.
2. Barton, R. W. and Neufeld, E. F. (1971) The Hurler corrective factor: purification andsome properties. Journal of Biological Chemistry, 246, 7773.
3. Crocker, A. C. (1972) Commentary: Plasma infusion therapy for Hurler’s syndrome. Pediatrics, 50, 683.
4. Danes, B. S. and Bearn, A. G. (1966) Hurler’s syndrome. A genetic study in cell culture. Journal of Experimental Medicine, 123, I.
5. Danes, B. S. and Bearn, A. G. (1967) Cellular metachromasia: a genetic marker for studying the mucopolysaccharidoses. Lancet, 1, 241.