Whole exon sequencing data from a patient with liddle syndrome

This is the data of whole exon sequencing of a newly-identified Liddle syndrome patient with a frameshift mutation in SCNN1B gene.本数据集为一名新确诊利德尔综合征（Liddle syndrome）患者的全外显子测序（whole exon sequencing）数据，该患者的SCNN1B基因（SCNN1B gene）存在移码突变。