1996•Nature GeneticsRequires access

Mice lacking both subunits of lysosomal β–hexosaminidase display gangliosidosis and mucopolysaccharidosis

Kazunori Sango, Michael P. McDonald, Jacqueline N. Crawley, Michelle L. Mack, Cynthia J. Tifft, Elisa Skop, Christopher M. Starr, Alexander Hoffmann, Konrad Sandhoff, Kinuko Suzuki, Richard L. Proia

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Key concepts: Sandhoff disease, HEXA, Gangliosidosis, Hexosaminidase, Biology, Mucopolysaccharidosis, Lysosomal storage disease, Tay-Sachs disease

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Mice lacking both subunits of lysosomal β–hexosaminidase display gangliosidosis and mucopolysaccharidosis — Research Paper | ScholarLens