Molecular pathology of Wilson's disease: a brief.

[1]  S. Nielsen,et al.  ATP7B copper-regulated traffic and association with the tight junctions: copper excretion into the bile. , 2008, Gastroenterology.

[2]  A. Taly,et al.  Withdrawal of penicillamine from zinc sulphate–penicillamine maintenance therapy in Wilson's disease: Promising, safe and cheap , 2008, Journal of the Neurological Sciences.

[3]  C. Wijmenga,et al.  Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. , 2007, Gastroenterology.

[4]  U. Shinde,et al.  Biochemical basis of regulation of human copper-transporting ATPases. , 2007, Archives of biochemistry and biophysics.

[5]  K. Ashkan,et al.  Wilson's disease , 2007, The Lancet.

[6]  H. Tsukahara,et al.  Relationship Between Oxidative Stress and Antioxidant Systems in the Liver of Patients With Wilson Disease: Hepatic Manifestation in Wilson Disease as a Consequence of Augmented Oxidative Stress , 2006, Pediatric Research.

[7]  P. Ferenci.  Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing , 2006, Human Genetics.

[8]  D. Cox,et al.  Copper-dependent trafficking of Wilson disease mutant ATP7B proteins. , 2000, Human molecular genetics.

[9]  J. Camakaris,et al.  A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network. , 1998, Human molecular genetics.

[10]  J. Rommens,et al.  The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene , 1993, Nature Genetics.

[11]  A. K. A. GIJSBERTI HODENPIJL.  [Wilson's disease]. , 1950, Maandschrift voor kindergeneeskunde.