Combined sialidase (neuraminidase) and β-galactosidase deficiency. Clinical, morphological and enzymological observations in a patient-Reference-Cited by-同舟云学术

Combined sialidase (neuraminidase) and β-galactosidase deficiency. Clinical, morphological and enzymological observations in a patient

Published:2008-04-23 Issue:2 Volume:26 Page:139-149
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Loonen M. C. B.,Reuser A. J. J.,Visser P.,Arts W. F. M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1984.tb00804.x/fullpdf

Reference38 articles.

1. Infantile neuraminidase and β-galactosidase deficiencies (galactosialidosis) with mild clinical courses;Andria;Perspectives in Inherited Metabolic Diseases,1981

2. Morquio-like syndrome with beta galactosidase deficiency and normal hexosaminesulfatase activity: mucopolysaccharidosis IVB;Arbisser;Am. J. Med. Genet.,1977

3. Molecular defect in combined β-galactosidase and neuraminidase deficiency in man;?Azzo;Proc. Nat. Acad. Sci. USA,1982

4. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes;Dodge;Arch. Biochem.,1963

5. Sialidosis (mucolipidosis I);Durand;Helv. Paediatr. Acta,1977

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