GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: A potential model for Tay Sachs disease-Reference-Cited by-同舟云学术

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GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: A potential model for Tay Sachs disease

Published:2013-01 Issue:1 Volume:108 Page:70-75
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Sanders Douglas N.,Zeng Rong,Wenger David A.,Johnson Gary S.,Johnson Gayle C.,Decker Jared E.,Katz Martin L.,Platt Simon R.,O'Brien Dennis P.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference39 articles.

1. The GM2 gangliosidoses;Gravel,2001

2. Biochemical consequences of mutations causing the GM2 gangliosidoses;Mahuran;Biochim. Biophys. Acta,1999

3. The GM2 activator protein, its roles as a co-factor in GM2 hydrolysis and as a general glycolipid transport protein;Mahuran;Biochim. Biophys. Acta,1998

4. GM2 gangliosidosis in a Japanese spaniel;Cummings;Acta Neuropathol.,1985

5. Enzyme alterations and lipid storage in three variants of Tay-Sachs disease;Sandhoff;J. Neurochem.,1971

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