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【摘 要】
：
Wilson’s disease(WD) is an autosomal recessive disorder of copper metabolism, caused by mutations in the ATP7 B gene. A clear demand for novel WD treatment str
【机 构】
：
DepartmentofTranslationalMedicalScience,TelethonInstituteofGeneticsandMedicine
【出 处】
：
世界胃肠病学杂志：英文版
【发表日期】
：
2017年30期
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