Utility of amniotic fluid chitotriosidase in the prenatal diagnosis of lysosomal storage disorders
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference31 articles.
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2. Plasma chitotriosidase activity in children with lysosomal storage disorders;Sheth;Indian J. Pediatr.,2010
3. Plasma chitotriosidase activity versus CCL18 level for assessing type I Gaucher disease severity: protocol for a systematic review with meta-analysis of individual participant data;Raskovalova;Syst. Rev.,2017
4. Cloning of a cDNA encoding chitotriosidase, a human chitinase produced by macrophages;Boot;J. Biol. Chem.,1995
5. Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease;Hollak;J. Clin. Invest.,1994
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