A mass spectrometric strategy for profiling glycoproteinoses, Pompe disease, and sialic acid storage diseases

Author:

Faid Valegh,Michalski Jean-Claude,Morelle Willy

Publisher

Wiley

Subject

Clinical Biochemistry

Reference69 articles.

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2. Normal and pathological catabolism of glycoproteins. in: , (Eds.) Glycoproteins and Disease. Elsevier Science BV, Amsterdam 1996, pp. 55–97.

3. Disorders of glycoprotein degradation: α-mannosidosis, β-mannosidosis, fucosidosis, and sialidosis. in: , , (Eds.) The Metabolic and Molecular Basis of Inherited Disease, McGraw-Hill, London 2001, pp. 3507–3533.

4. Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture

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