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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 4, 2024. (Total: 234082Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Hepatolenticular Degeneration and ATP7B[original query]
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
[Analysis of clinical and genetic characteristics of the severe liver disease phenotype in patients with hepatolenticular degeneration].
Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2024 7 32 (6): 551-557.
Q Q Xiao, Y H Xu, X Xu, Y W Shi, H X Cao, X Q Liu, J G F
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