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Abstract

GM2 gangliosidosis is a fatal, progressive neuronopathic lysosomal storage disease resulting from a deficiency of β-N-acetylhexosaminidase (EC 3.2.1.52) activity. GM2 gangliosidosis occurs with varying degrees of severity in humans and in a variety of animals, including cats. In the current...

Author(s)
Bradbury, A. M.; Morrison, N. E.; Hwang, M.; Cox, N. R.; Baker, H. J.; Martin, D. R.
Publisher
Academic Press, Orlando, USA
Citation
Molecular Genetics and Metabolism, 2009, 97, 1, pp 53-59