Tetrathiomolybdate in the treatment of acute hepatitis in an animal model for Wilson disease

The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene

Peter C. Bull, Gordon R. Thomas, Johanna M. Rommens et al. · Nature Genetics · 1993 · 1.9K citations

Wilson Disease Gene, Genetics, Pathogenesis +7

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Rudolph E. Tanzi, Konstantin Petrukhin, Jean‐Luc Pellequer et al. · Nature Genetics · 1993 · 1.4K citations

Mendelian Disorder, Disease Mechanism, Wilson Disease Gene +11

A Practice Guideline on Wilson Disease

Eve A. Roberts, Michael L. Schilsky · Hepatology · 2003 · 452 citations · Full text

Clinical Finding, Disease Mechanism, Pathogenesis +4

The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene

Jingshi Wu, John Forbes, Hai Shiene Chen et al. · Nature Genetics · 1994 · 385 citations

Molecular Physiology, Biochemistry, Mitochondrial Function +10

Worsening of Neurologic Syndrome in Patients With Wilson's Disease With Initial Penicillamine Therapy

George J. Brewer, Colin Terry, Alex M. Aisen et al. · Archives of Neurology · 1987 · 334 citations

Neurologic Syndrome, Corticobasal Degeneration, Neurological Disorder +16