Article

Mutations in<i>ZBTB20</i>in individuals with persistent stuttering

2022-11-07

Abstract excerpt

<h4>Background</h4> Previous studies identified a strong linkage signal for non-syndromic persistent developmental stuttering on chromosome 3q13.2-3q13.33 in a large consanguineous family. To identify the causative genetic variant at this locus, including we performed further analysis, including whole exome, whole genome, and targeting Sanger sequencing. <h4>Results</h4> We identified a homozygous rare c.2155G>A v...

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Literature Corpus work: db79040d-e766-5ce6-97b9-107b53683aba
DOI: 10.1101/2022.11.03.22281471

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