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7. Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patient. Kok KF; Hoevenaars B; Waanders E; Drenth JP Neth J Med; 2008 Sep; 66(8):348-50. PubMed ID: 18809983 [TBL] [Abstract][Full Text] [Related]
16. A genetic study of Wilson's disease in the United Kingdom. Coffey AJ; Durkie M; Hague S; McLay K; Emmerson J; Lo C; Klaffke S; Joyce CJ; Dhawan A; Hadzic N; Mieli-Vergani G; Kirk R; Elizabeth Allen K; Nicholl D; Wong S; Griffiths W; Smithson S; Giffin N; Taha A; Connolly S; Gillett GT; Tanner S; Bonham J; Sharrack B; Palotie A; Rattray M; Dalton A; Bandmann O Brain; 2013 May; 136(Pt 5):1476-87. PubMed ID: 23518715 [TBL] [Abstract][Full Text] [Related]
17. [Expression characters of ATP7B mRNA in liver tissue of patients with Wilson's disease]. Shi Z; Li XH; Wang Y; Liang XL Zhonghua Gan Zang Bing Za Zhi; 2003 Feb; 11(2):99. PubMed ID: 12648406 [No Abstract] [Full Text] [Related]
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19. Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence? Battisti C; Dotti MT; Loudianos G; Dessì V; Battistini S; Amato T; Rufa A; Federico A Neurol Sci; 2004 Apr; 25(1):18-20. PubMed ID: 15060811 [TBL] [Abstract][Full Text] [Related]
20. Direct sequencing of mutations in the copper-transporting P-type adenosine triphosphate (ATP7B) gene for diagnosis and pathogenesis of Wilson's disease. Zhang DF; Teng JF Genet Mol Res; 2016 Sep; 15(3):. PubMed ID: 27706781 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]