Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Hepatolenticular Degeneration and ATP7B[original query] |
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Direct sequencing of mutations in the copper-transporting P-type adenosine triphosphate (ATP7B) gene for diagnosis and pathogenesis of Wilson's disease. Genetics and molecular research : GMR 2016 Sep 15 (3): . Zhang D F, Teng J |
Analysis and application of ATP7B gene mutations in 35 patients with hepatolenticular degeneration. Genetics and molecular research : GMR 2015 14 (4): 18764-70. Zong Y N, Kong X |
[Mutational analysis of ATP7B gene of hepatolenticular degeneration in Xinjiang region]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2020 9 28 (8): 699-702. Aerziguli Aierken, Li C Z, Hu L H, Lu X B, Sun X |
Case Report: The First Reported Concurrence of Wilson Disease and Bilateral Retinitis Pigmentosa. Frontiers in medicine 2022 5 9 877752. Ye Zifan, Jia Xiuhua, Liu Xin, Zhang Qi, Wang Kaijun, Chen M |
[Management of hepatolenticular degeneration during pregnancy]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2022 2 30 (1): 107-109. Bai J, Zheng S J, Duan Z |
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- Page last updated:Nov 28, 2023
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