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2012•Molecular Genetics and MetabolismRequires access

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

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

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Key concepts: Gangliosidosis, HEXA, Hexosaminidase, Tay-Sachs disease, Sandhoff disease, Missense mutation, Chemistry, Molecular biology

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