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

Authors: Hund E.; Grau A.; Fogel W.; Forsting M.; Cantz M.; Kustermann-Kuhn B.; Harzer K.; Navon R.; Goebel H.H.; Meinck H.-M.

Source: Journal of the Neurological Sciences, Volume 145, Number 1, January 1997 , pp. 25-31(7)

Publisher: Elsevier

Keywords: G_M2 gangliosidosis; Hexosaminidase; Tay-Sachs disease; Ataxia; Weakness; Motor neuron disease; Spinal muscular atrophy

Language: English

Document Type: Research article

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

Affiliations: 1: Department of Neurology, University of Heidelberg, Im Neuenheimer Feld 400, D-69120 Heidelberg, Germany

Publication date: 1997-01-01

• In this: publication
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• In this Subject: Neurology & Psychiatry
• By this author: Hund E. ;  Grau A. ;  Fogel W. ;  Forsting M. ;  Cantz M. ;  Kustermann-Kuhn B. ;  Harzer K. ;  Navon R. ;  Goebel H.H. ;  Meinck H.-M.

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