Biochemical basis of six different types of sialidosis
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(78)81239-3/fullpdf
Reference22 articles.
1. I-Cell Disease: Biochemical Studies
2. Structure of the three major sialyl-oligosaccharides excreted in the urine of five patients with three distinct inborn diseases: “I cell disease” and two new types of mucolipidosis
3. Structure of Nine Sialyl-Oligosaccharides Accumulated in Urine of Eleven Patients with Three Different Types of Sialidosis. Mucolipidosis II and Two New Types of Mucolipidosis
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1. Glycolipid and Glycoprotein Degradation;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22
2. Severe Infantile Sialidosis-The Characteristics of Oligosaccharides Isolated from the Urine and the Abdominal Ascites.;The Tohoku Journal of Experimental Medicine;1992
3. NOVEL LYSOSOMAL GLYCOAMINOACID STORAGE DISEASE WITH ANGIOKERATOMA CORPORIS DIFFUSUM;The Lancet;1989-04
4. Specificity studies on the oligosaccharide neuraminidase of human fibroblasts;Biochemical Journal;1984-03-01
5. Angeborene Stoffwechselkrankheiten;Pathologie;1984
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