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)
创建时间：
2018-05-03
