Morquio B syndrome: A primary defect in β-galactosidase-Reference-Cited by-同舟云学术

Morquio B syndrome: A primary defect in β-galactosidase

Published:1983-10 Issue:2 Volume:16 Page:261-275
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

van der Horst Gijsbertus T. J.,Kleijer Wim J.,Hoogeveen André T.,Huijmans Jan G. M.,Blom Wim,van Diggelen Otto P.

Publisher

Wiley

Subject

Genetics (clinical)

Reference41 articles.

1. Two-dimensional electrophoresis of urinary mucopolysaccharides on cellulose acetate after f-cetylpyridiniumchloride (CPC) precipitation: A method suitable for the routine laboratory

2. (1981): Infantile neuraminidase and β-galactosidase deficiencies (galactosialidosis) with mild clinical courses. In (ed): “Perspectives in Inherited Metabolic Diseases 4.” Milano, Italy: 379-395.

3. Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: Mucopolysaccharidosis IVB

4. In situ detection of mycoplasma contamination in cell cultures by fluorescent Hoechst 33258 stain

5. Molecular defect in combined beta-galactosidase and neuraminidase deficiency in man.

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