The laboratory diagnosis of sanfilippo disease
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference20 articles.
1. Mental retardation associated with acid mucopolysacchariduria (heparitin sulfate type)
2. Biochemical heterogeneity of the sanfilippo syndrome: Preliminary characterization of two deficient factors
3. The Sanfilippo A Corrective Factor
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1. Coinheritance of novel mutations in NAGLU causing mucopolysaccharidosis type IIIB and in DDHD2 causing spastic paraplegia54 in a Turkish family;Journal of Clinical Neuroscience;2020-12
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