Progressive cerebellar ataxia, proximal neurogenic weakness and ocular motor disturbances: hexosaminidase A deficiency with late clinical onset in four siblings

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Keywords: Ataxia; GM2 gangliosidosis; Hexosaminidase; Motor neuron disease; Spinal muscular atrophy; Tay-Sachs disease; Weakness

Document Type: Research Article

DOI: http://dx.doi.org/10.1016/S0022-510X(96)00233-X

Affiliations: Department of Neurology, University of Heidelberg, Im Neuenheimer Feld 400, D-69120 Heidelberg, Germany

Publication date: January 1, 1997

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