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Article

IFNAR1 gene mutation may contribute to developmental stuttering in the Chinese population.

Hereditas - 18 Nov 2021

Sun Yimin, Gao Yong, Zhou Yuxi, Zhou Yulong, Zhang Ying, Wang Dong, Tan Li-Hai

Abstract excerpt

BACKGROUND: Developmental stuttering is the most common form of stuttering without apparent neurogenic or psychogenic impairment. Recently, whole-exome sequencing (WES) has been suggested to be a promising approach to study Mendelian disorders. METHODS: Here, we describe an application of WES to identify a gene potentially responsible for persistent developmental stuttering (PDS) by sequencing DNA samples from 10...

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PMID: 34794508
DOI: 10.1186/s41065-021-00211-y
PMCID: PMC8600687

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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