A common mutation for mucopolysaccharidosis type I associated with a severe Hurler syndrome phenotype
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference28 articles.
1. The Defect in the Hurler and Scheie Syndromes: Deficiency of -L-Iduronidase
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3. Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state.
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