Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VI-Reference-Cited by-同舟云学术

Clinical and biochemical study of 28 patients with mucopolysaccharidosis type VI

Published:2004-06-25 Issue:3 Volume:66 Page:208-213
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Azevedo ACMM,Schwartz IV,Kalakun L,Brustolin S,Burin MG,Beheregaray APC,Leistner S,Giugliani C,Rosa M,Barrios P,Marinho D,Esteves P,Valadares E,Boy R,Horovitz D,Mabe P,Da Silva LCS,De Souza ICN,Ribeiro M,Martins AM,Palhares D,Kim CA,Giugliani R

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00277.x/fullpdf

Reference23 articles.

1. Replacement therapy in Mucopolysaccharidosis type VI: advantages of early onset of therapy

2. Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase

3. Phylogenetic conservation of arylsulfatases. cDNA cloning and expression of human arylsulfatase B.

4. Mucopolysaccharidosis Type VI (Maroteaux−Lamy Syndrome): A Y210C Mutation Causes either Altered Protein Handling or Altered Protein Function of N-Acetylgalactosamine 4-Sulfatase at Multiple Points in the Vacuolar Network

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