Additional file 1: Table S1. of A novel KCNQ1 nonsense variant in the isoform-specific first exon causes both jervell and Lange-Nielsen syndrome 1 and long QT syndrome 1: a case report

Name: Additional file 1: Table S1. of A novel KCNQ1 nonsense variant in the isoform-specific first exon causes both jervell and Lange-Nielsen syndrome 1 and long QT syndrome 1: a case report
Creator: Marehiko Ueda
Published: 2017-06-09 00:00:00
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Figshare2017-06-09 更新2026-04-08 收录

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https://springernature.figshare.com/articles/dataset/Additional_file_1_Table_S1_of_A_novel_KCNQ1_nonsense_variant_in_the_isoform-specific_first_exon_causes_both_jervell_and_Lange-Nielsen_syndrome_1_and_long_QT_syndrome_1_a_case_report/5096770/1

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The probandâ s (II-2 in Fig. 2) results of genetic screening of LQT causative genes (KCNQ1, KCNH2, SCN5A, KCNE1, KCNE2, KCNJ2, SCN4B, KCNJ5). Entire coding exons, including the intronic boundaries of the genes were analyzed. (XLSX 10 kb)

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Marehiko Ueda

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2017-06-09