Roberts EA, Schilsky ML (7 September 2023). "Current and Emerging Issues in Wilson's Disease". New England Journal of Medicine. 389 (10): 922–938. doi:10.1056/NEJMra1903585. PMID37672695. S2CID261581755.
Cumings JN (1948). "The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration". Brain. 71 (Dec): 410–15. doi:10.1093/brain/71.4.410. PMID18124738.
McIntyre N, Clink HM, Levi AJ, Cumings JN, Sherlock S (February 1967). "Hemolytic anemia in Wilson's disease". N. Engl. J. Med. 276 (8): 439–44. doi:10.1056/NEJM196702232760804. PMID6018274.
Cumings JN (March 1951). "The effects of B.A.L. in hepatolenticular degeneration". Brain. 74 (1): 10–22. doi:10.1093/brain/74.1.10. PMID14830662.
Denny-Brown D, Porter H (December 1951). "The effect of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease)". N. Engl. J. Med. 245 (24): 917–25. doi:10.1056/NEJM195112132452401. PMID14882450.
Vilensky JA, Robertson WM, Gilman S (September 2002). "Denny-Brown, Wilson's disease, and BAL (British antilewisite [2,3-dimercaptopropanol])". Neurology. 59 (6): 914–16. doi:10.1212/wnl.59.6.914. PMID12297577.
Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW (1993). "The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene". Nat. Genet. 5 (4): 327–37. doi:10.1038/ng1293-327. PMID8298639. S2CID1236890.
Tanzi RE, Petrukhin K, Chernov I, et al. (1993). "The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene". Nat. Genet. 5 (4): 344–50. doi:10.1038/ng1293-344. PMID8298641. S2CID610188.
Müller T, van de Sluis B, Zhernakova A, et al. (2003). "The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis". J. Hepatol. 38 (2): 164–68. doi:10.1016/S0168-8278(02)00356-2. PMID12547404.
Pandey N, John S (21 June 2022). "Kayser-Fleischer Ring". StatPearls. Treasure Island, Florida: StatPearls Publishing. PMID29083643. Retrieved 30 November 2022.
Roberts EA, Schilsky ML (7 September 2023). "Current and Emerging Issues in Wilson's Disease". New England Journal of Medicine. 389 (10): 922–938. doi:10.1056/NEJMra1903585. PMID37672695. S2CID261581755.
Cumings JN (1948). "The copper and iron content of brain and liver in the normal and in hepato-lenticular degeneration". Brain. 71 (Dec): 410–15. doi:10.1093/brain/71.4.410. PMID18124738.
McIntyre N, Clink HM, Levi AJ, Cumings JN, Sherlock S (February 1967). "Hemolytic anemia in Wilson's disease". N. Engl. J. Med. 276 (8): 439–44. doi:10.1056/NEJM196702232760804. PMID6018274.
Cumings JN (March 1951). "The effects of B.A.L. in hepatolenticular degeneration". Brain. 74 (1): 10–22. doi:10.1093/brain/74.1.10. PMID14830662.
Denny-Brown D, Porter H (December 1951). "The effect of BAL (2,3-dimercaptopropanol) on hepatolenticular degeneration (Wilson's disease)". N. Engl. J. Med. 245 (24): 917–25. doi:10.1056/NEJM195112132452401. PMID14882450.
Vilensky JA, Robertson WM, Gilman S (September 2002). "Denny-Brown, Wilson's disease, and BAL (British antilewisite [2,3-dimercaptopropanol])". Neurology. 59 (6): 914–16. doi:10.1212/wnl.59.6.914. PMID12297577.
Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW (1993). "The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene". Nat. Genet. 5 (4): 327–37. doi:10.1038/ng1293-327. PMID8298639. S2CID1236890.
Tanzi RE, Petrukhin K, Chernov I, et al. (1993). "The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene". Nat. Genet. 5 (4): 344–50. doi:10.1038/ng1293-344. PMID8298641. S2CID610188.
Müller T, van de Sluis B, Zhernakova A, et al. (2003). "The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis". J. Hepatol. 38 (2): 164–68. doi:10.1016/S0168-8278(02)00356-2. PMID12547404.
Pandey N, John S (21 June 2022). "Kayser-Fleischer Ring". StatPearls. Treasure Island, Florida: StatPearls Publishing. PMID29083643. Retrieved 30 November 2022.
Roberts EA, Schilsky ML (7 September 2023). "Current and Emerging Issues in Wilson's Disease". New England Journal of Medicine. 389 (10): 922–938. doi:10.1056/NEJMra1903585. PMID37672695. S2CID261581755.
Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW (1993). "The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene". Nat. Genet. 5 (4): 327–37. doi:10.1038/ng1293-327. PMID8298639. S2CID1236890.
Tanzi RE, Petrukhin K, Chernov I, et al. (1993). "The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene". Nat. Genet. 5 (4): 344–50. doi:10.1038/ng1293-344. PMID8298641. S2CID610188.