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

Name: 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
Creator: Zamzureena Mohd Rani; Pei-Sin Chong; Nor Azian Abdul Murad; Jia-Shiun Khoo; Loo-Ling Wu; Yock-Ping Chow
Published: 2017-03-10 00:00:00
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Figshare2017-03-10 更新2026-04-08 收录

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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

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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：

Zamzureena Mohd Rani; Pei-Sin Chong; Nor Azian Abdul Murad; Jia-Shiun Khoo; Loo-Ling Wu; Yock-Ping Chow

创建时间：

2017-02-22