Suggested Reading

Cleveland, D. W. (1999). From charcot to SOD1: Mechanisms of selective motor neuron death in ALS. Neuron 24, 515-520.

Cudkowicz, M. E., McKenna-Yasek, D., Sapp, P. E., Chin, W., Geller, B., Hayden, D. L., Schoenfeld, D. A., Hosler, B. A., Horvitz, H. R., and Brown, R. H. (1997). Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis. Ann. Neurol. 41, 210-221.

Culotta, V. C., Lin, S. J., Schmidt, P., Klomp, L. W., Casareno, R. L., and Gitlin, J. (1999). Intracellular pathways of copper trafficking in yeast and humans. Adv. Exp. Med. Biol. 448, 247254.

Fischbeck, K. H.,Lieberman, A., Bailey, C. K., Abel, A., and Merry, D. E. (1999). Androgen receptor mutation in Kennedy's disease. Philos. Trans. R Soc. London B Biol. Sci. 354, 1075.

The Hereditary Spastic Paraplegia Working Group. Hereditary spastic paraplegia: Advances in genetic research. Neurology 46, 1507-1514.

Julien, J.-P. (1999). Neurofilament functions in health and disease. Curr. Opin. Neurobiol. 9, 554-560.

Lee, V. M. Y., and Trojanowski, J. Q. (1999). Neurodegenerative taupathies: Human disease and transgenic mouse models. Neuron 24, 507-510.

Lefebvre, S., Burglen, L., Frezal, J., Munnich, A., and Melki, J. (1998). The role of the SMN gene in proximal spinal muscular atrophy. Hum. Mol. Genet. 7, 1531-1536.

Patel, S., and Latterich, M. (1998). The AAA team: Related ATPases with diverse functions. Trends Cell Biol. 8, 65-71.

Price, D. L., Sisodia, S. S., and Borchelt, D. R. (1998). Genetic neurodegenerative diseases: The human illness and transgenic models. Science 282, 1079-1083.

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