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In silico analysis of the CIB2: c.556C>T (p.Arg186Trp) mutation.

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Figshare2015-12-03 更新2026-04-29 收录
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https://figshare.com/articles/dataset/_A_Novel_C_Terminal_CIB2_Calcium_and_Integrin_Binding_Protein_2_Mutation_Associated_with_Non_Syndromic_Hearing_Loss_in_a_Hispanic_Family_/1562040
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资源简介:
We performed a bioinformatic analysis of the c.556C>T mutation in CIB2 to determine its predicted pathogenicity. We provide the SNP ID number from dbSNP, frequency of occurrence in European and African American populations as well as results from pathogenicity predication software. (DOCX)
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2015-12-03
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