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

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

Abstract 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...

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Bibliographic Details
Main Authors: Yimin Sun, Yong Gao, Yuxi Zhou, Yulong Zhou, Ying Zhang, Dong Wang, Li-Hai Tan
Format: Article
Language:English
Published: BMC 2021-11-01
Series:Hereditas
Subjects:
IFNAR1
Developmental stuttering
Whole-exome sequencing (WES)
Persistent developmental stuttering (PDS)
Online Access:https://doi.org/10.1186/s41065-021-00211-y

Internet

https://doi.org/10.1186/s41065-021-00211-y

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