Validation of disaccharide compositions derived from dermatan sulfate and heparan sulfate in mucopolysaccharidoses and mucolipidoses II and III by tandem mass spectrometry

Author:

Tomatsu Shunji,Montaño Adriana M.,Oguma Toshihiro,Dung Vu Chi,Oikawa Hirotaka,Gutiérrez María L.,Yamaguchi Seiji,Suzuki Yasuyuki,Fukushi Masaru,Barrera Luis A.,Kida Kazuhiro,Kubota Mitsuru,Orii Tadao

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference48 articles.

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2. I-cell disease and pseudo-Hurler polydystrophy: disorders of lysosomal enzyme phosphorylation and localization;Kornfeld,2001

3. Clinical, biochemical and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture;Tondeur;J. Pediatr.,1971

4. I-cell disease: multiple lysosomal-enzyme defect;Lightbody;Lancet,1971

5. Prevalence of lysosomal storage disorders;Meikle;JAMA,1999

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