Diagnosis of patients with mucopolysaccharidosis type II via RNA sequencing
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference30 articles.
1. Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment;D’Avanzo;Int J Mol Sci.,2020
2. Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy;Wraith;Eur J Pediatr.,2008
3. Natural progression of neurological disease in mucopolysaccharidosis type II;Holt;Pediatrics.,2011
4. Management of the behavioural manifestations of Hunter syndrome;Roberts;Br J Nurs.,2016
5. Diagnosing lysosomal storage disorders: mucopolysaccharidosis type II;Johnson;Curr Protoc Hum Genet.,2013
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