The ATP7B c.3316 G > A variant is associated with mild subphenotype in Wilson disease: a single-center cohort study
ATP7B c.3316 G > A 变异与威尔逊病轻型亚表型相关:一项单中心队列研究
期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-026-04259-9
Liu, Lisheng; Fang, Mingjuan; Ai, Wenlong; Shu, Shan; Zhao, Wen; Yan, Yan; Cheng, Nan; Hu, Wenbin; Xu, Yin