Additional file 4: Table S3. of Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family
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https://springernature.figshare.com/articles/dataset/Additional_file_4_Table_S3_of_Exome_sequencing_identifies_SLC26A4_GJB2_SCARB2_and_DUOX2_mutations_in_2_siblings_with_Pendred_syndrome_in_a_Malaysian_family/4680256/1
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资源简介：
List of other possible PDS causal mutations which uniquely inherited by the eldest sister. (XLSX 11 kb)
提供机构：
Figshare
创建时间：
2017-12-18
