S. La Fontaine

Publication List Details

Period

2001 - 2001

Number

1

Co-Authors

Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copperATPase (2001)

La Fontaine, S., Theophilos, M. B., Firth, S. D., Gould, R., Parton, R. G., Mercer, J. F. B.

Wilson disease is an autosomal recessive copper transport disorder resulting from defective biliary excretion of copper and subsequent hepatic copper accumulation and liver failure if not treated....