Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case-Reference-Cited by-同舟云学术

Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further case

Published:2008-04-23 Issue:3 Volume:18 Page:203-210
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Winter RobinM.,Swallow DallasM.,Baraitser Michael,Purkiss Paul

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1980.tb00873.x/fullpdf

Reference27 articles.

1. Acid hydrolase deficiencies and abnormal glycoproteins in mucolipidosis III (pseudo-Hurler polydystrophy);Berman;Clin. chim. Acta,1974

2. Sialidosis (mucolipidosis 1);Durand;Helv. Paediat. Acta,1977

3. Two siblings with mucolipidosis;Fukunaga;Clin. Neurol. (Tokyo),1976

4. Infantile sialidosis: A phenocopy of GMI gangliosidosis distinguished by genetic complementation and urinary oligosaccharides;Gravel;Amer. J. hum. Genet.,1979

5. Separation of glycoprotein-derived oligosaccharides by thin-layer chromatography;Holmes;Anal. Biochem.,1978

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