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R778L和P992L复合突变致肝豆状核变性2例

Two cases of hepatolenticular degeneration caused by combined R778L and P992L mutation
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摘要 肝豆状核变性发病隐匿,临床表现多样,易被漏诊、误诊。现报道2例未成年女性肝豆状核变性患者,并对患者及其家系行ATP7B基因外显子测序,进行相关文献复习,以期进一步了解该罕见病的基因特点。
作者 程齐齐 杨丽霞 徐清浪 鄢秀华 邬小萍 葛善飞 Cheng Qiqi;Yang Lixia;Xu Qinglang;Yan Xiuhua;Wu Xiaoping;Ge Shanfei(Department of Infectious Diseases,The First Affiliated Hospital of Nanchang University,Nanchang 330006,China;Department of Infectious Diseases,Shangrao Second People's Hospital,Shangrao 334000,China)
出处 《中华肝脏病杂志》 CSCD 北大核心 2021年第12期1201-1204,共4页 Chinese Journal of Hepatology
基金 国家自然科学基金地区基金项目 (81660109)。
关键词 肝豆状核变性 基因检测 复合突变 ATP7B Hepatolenticular degeneration Genetic testing Combined mutation ATP7B
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