Enzymatic diagnosis of the mucopolysaccharidoses Experience of 96 cases diagnosed in a five‐year period

Author:

Hopwood John J.1,Muller Vivienne1,Harrison John R.1,Carey William F.1,Elliott Helen1,Robertson Evelyn F.1,Pollard Anthony C.1

Affiliation:

1. Department of Chemical PathologyThe Adelaide Children's HospitalKing William RoadNorth AdelaideSA5006

Publisher

AMPCo

Subject

General Medicine

Reference25 articles.

1. Sanfilippo disease type D: deficiency of N-acetylglucosamine-6-sulfate sulfatase required for heparan sulfate degradation.

2. Diagnosis of Gaucher's Disease and Niemann-Pick Disease with Small Samples of Venous Blood

3. High resolution electrophoresis of urinary glycosaminoglycans: an improved screening test for the mucopolysaccharidoses;Hopwood JJ;Anal Biochem,1981

4. X‐L‐iduronidase. β‐D‐glucuronidase and 2‐sulfo‐L‐iduronate 2‐sulfatase: preparation and characterization of radioactive substrates from heparin;Hopwood JJ;C'arhohydr Res,1969

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