Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and α1-antitrypsin deficiencydeficiency-Reference-Cited by-同舟云学术

Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and α1-antitrypsin deficiencydeficiency

Published:1986-12 Issue:6 Volume:145 Page:572-575
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Nielsen J. B.,Güttler F.,Hobolth N.,Tønnesen T.,Pedersen O. D.,Lykkelund C.,Rosleff F.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF02429071.pdf

Reference20 articles.

1. Blom M, Hjørne M (1976) Profile analysis of blood proteins with a centrifugal analyzer. Clin Chem 22:657–662

2. Blumenkrantz N, Asboe-Hansen G (1973) New method for quantitative determination of uronic acids. Anal Biochem 54:484–489

3. Childs B, Der Kaloustian V (1968) Genetic heterogeneity. N Engl J Med 279:1205–1212

4. Cook PJL (1975) The genetics of α1-antitrypsin. A family study in England and Scotland. Ann Hum Genet 38:275–287

5. Di Ferrante N, Neri G, Neri ME, Hogsett WE (1972) Measurement of urinary glycosaminoglycans with quaternary ammonium salts: an extension of the method. Connect Tissue Res 1:93–101

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