Analysis of the IDS Gene in 38 Patients with Hunter Syndrome: The c.879G>A (p.Gln293Gln) Synonymous Variation in a Female Create Exonic Splicing
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference36 articles.
1. Presence of an IDS-related locus (IDS2) in Xq28 complicates the mutational analysis of Hunter syndrome.;ML Bondeson;Eur J Hum Genet,1995
2. Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome.;ML Bondeson;Hum Mol Genet,1995
3. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).;R Martin;Pediatrics,2008
4. Mild and severe Hunter syndrome (MPS II) within the same sibships.;S Yatziv;Clin Genet,1977
5. Incidence of mucopolysaccharidoses in Israel: is Hunter disease a “Jewish disease”?;T Schaap;Hum Genet,1980
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