Detection of hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: Biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers-Reference-Cited by-同舟云学术

Detection of hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: Biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers

Published:2006-07 Issue:1 Volume:369 Page:29-34
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Lin Shuan-Pei,Chang Jui-Hung,Lee-Chen Guey-Jen,Lin Dar-Shong,Lin Hsiang-Yu,Chuang Chih-Kuang

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference18 articles.

1. The mucopolysaccharidoses;Neufeld,1995

2. Mucopolysaccharidosis and mucolipidosis;Lin,2004

3. Mutational spectrum of the iduronate 2 sulfatase gene in 25 unrelated Korean Hunter syndrome patients: identification of 13 novel mutations;Kim;Hum Mutat,2003

4. Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II;Kato;J Hum Genet,2005

5. Sequence of the human iduronate 2-sulfatase (IDS) gene;Wilson;Genomics,1993

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