I-Cell disease (Mucolipidosis II)

Author:

Martin J. J.,Leroy J. G.,Farriaux J. P.,Fontaine G.,Desnick R. J.,Cabello A.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Reference38 articles.

1. Antonopoulos, C. A., Borelius, E., Gardell, S., Hamnstr�m, B., Scott, J. E.: The precipitation of polyanions by long-chain aliphatic ammonium copounds: IV. Elution in salt solutions of mucopolysaccharide-quaternary ammonium complexes adsorbed on a support. Biochim. biophys. Acta (Amst.)54, 213?226 (1961)

2. Belcher, R. W.: Ultrastructure of the skin in the genetic mucopolysaccharidoses. Arch. Path.94, 511?518 (1972)

3. Belcher, R. W.: Ultrastructure and function of eccrine glands in the mucopolysaccharidoses. Arch. Path.96, 339?341 (1973)

4. Blank, E., Linder, D.: I-cell disease (Mucolipidosis II): a lysosomopathy. Pediatrics54, 797?805 (1974)

5. Cowen, D., Olmstead, E. V.: Infantile neuroaxonal dystrophy. J. Neuropath. exp. Neurol.22, 175?236 (1963)

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4. The Pathology of the Skeleton in Lysosomal Storage Diseases;Pathobiology of Human Disease;2014

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