Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 28, 2023. (Total: 223416Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 5 (of 5 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
TOP