Biology and potential strategies for the treatment of GM2 gangliosidoses

Author:

Chavany Christine,Jendoubi Moncef

Publisher

Elsevier BV

Subject

Genetics,Molecular Medicine

Reference36 articles.

1. The biochemistry of HEXA and HEXB gene mutations causing GM2 gangliosidosis;Mahuran;Biochim. Biophys. Acta,1991

2. Formation of a ternary complex between GM2 activator protein, GM2 ganglioside and hexosaminidase A;Yadao;Biochim. Biophys. Acta,1997

3. Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis;Sango;Nat. Genet.,1996

4. Sandhoff, K. et al. (1989) The GM2 gangliosidoses, in The Metabolic Basis of Inherited Disease (Scriver, C.V., Beaudet, A.L., Sly, W.S. and Valle, D., eds), pp. 1807–1839, McGraw-Hill

5. Gravel, R.A. (1995) The GM2 gangliosidoses, in The Metabolic and Molecular Basis of Inherited Disease (Scriver, C.R., Beaudet, A.L., Sly, W.S. and Valle, D., eds), pp. 2839–2879, McGraw-Hill

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