(转化医学国家重大科技基础设施 北京协和)-北京市东城区帅府园一号,100730
(疑难重症及罕见病全国重点实验室)-北京市大兴区榆垡镇今荣大街73号,102602
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Liu C, Gong Y*, Xia W*, et al. Defective O-glycosylation of novel FGF23 mutations in a Chinese family with hyperphosphatemic familial tumoral calcinosis. Bone, 2020, 137:115401.
文章链接:http://linkinghub.elsevier.com/retrieve/pii/S8756-3282(20)30181-2