Sandhoff Disease: Defective Glycosaminoglycan Catabolism in Cultured Fibroblasts and Its Correction by beta-N-Acetylhexosaminidase-Reference-Cited by-同舟云学术

Sandhoff Disease: Defective Glycosaminoglycan Catabolism in Cultured Fibroblasts and Its Correction by beta-N-Acetylhexosaminidase

Published:1974-09 Issue:3 Volume:47 Page:581-590
ISSN:0014-2956
Container-title:European Journal of Biochemistry
language:en
Short-container-title:Eur J Biochem

Author:

CANTZ Michael,KRESSE Hans

Publisher

Wiley

Subject

Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1974.tb03729.x/fullpdf

Reference44 articles.

1. 1. H. R. Sloan, D. S. Fredrickson, J. B. Stanbury, J. B. Wyngaarden, and D. S. Fredrickson (1972 ) inThe Metabolic Basis of Inherited Disease () 3rd edn , pp.615 -638 , McGraw-Hill Inc., New York.

2. Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs

3. Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

4. N-ACETYLHEXOSAMINIDASE ACTIVITIES IN TAY-SACHS DISEASE

5. Variation of β-N-acetylhexosaminidase-pattern in Tay-Sachs disease

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