2例钠牛磺胆酸共转运多肽缺陷病患儿临床分析(4)
[12] Liu R,Chen C,Xia X,et al. Homozygous p.Ser267phe in SLC10A1 is associated with a new type of hypercholanemia and implications for personalized medicine[J]. Sci Rep,2017,7(1):9214.[13] 宋元宗.钠牛磺胆酸共转运多肽缺陷病的发病机制、临床表现及诊疗进展[J].临床肝胆病杂志 ......
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