Additional file 2: of A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report
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Table S2. Exonic variants in the TG gene identified in the proposita by whole exome sequencing. All exonic variants in the TG gene identified in the proposita. (XLSX 41Â kb)
表S2：通过全外显子组测序（whole exome sequencing）在先证者（proposita）中鉴定出的TG基因外显子变异。本数据集包含通过全外显子组测序在先证者中鉴定出的全部TG基因外显子变异。（XLSX 41 KB）
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figshare创建时间：
2018-05-03
