IFNAR1 gene mutation may contribute to developmental stuttering in the Chinese population
IFNAR1 gene mutation may contribute to developmental stuttering in the Chinese population
About this item
Full title
Author / Creator
Sun, Yimin , Gao, Yong , Zhou, Yuxi , Zhou, Yulong , Zhang, Ying , Wang, Dong and Tan, Li-Hai
Publisher
England: Springer
Journal title
Language
English
Formats
Publication information
Publisher
England: Springer
Subjects
More information
Scope and Contents
Contents
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.
Here, we describe an application of WES to identify a gene potentially responsible for persistent developmental st...
Alternative Titles
Full title
IFNAR1 gene mutation may contribute to developmental stuttering in the Chinese population
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_e273dcdf35b64e959c8b8b3d205cc06a
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_e273dcdf35b64e959c8b8b3d205cc06a
Other Identifiers
ISSN
1601-5223,0018-0661
E-ISSN
1601-5223
DOI
10.1186/s41065-021-00211-y
