diagnosis of Sandhoff's disease
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference18 articles.
1. Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs
2. ENZYME ALTERATIONS AND LIPID STORAGE IN THREE VARIANTS OF TAY-SACHS DISEASE
3. Sandhoff, K., in Enzyme Therapy in Genetic Diseases, R. J. Desnick, R. W. Bernlohr, and W. Krivit, Eds., National Foundation, New York, in press.
4. GM2-gangliosidosis with total hexosaminidase deficiency
5. Generalized accumulation of neutral glycosphingolipids with GM2 ganglioside accumulation in the brain
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