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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https://springernature.figshare.com/articles/Additional_file_2_of_A_novel_mutation_in_the_TG_gene_G2322S_causing_congenital_hypothyroidism_in_a_Sudanese_family_a_case_report/6214478/1
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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)
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figshare
创建时间：
2018-05-03
