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

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 ide...

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Detalles Bibliográficos
Autores principales: Sun, Yimin, Gao, Yong, Zhou, Yuxi, Zhou, Yulong, Zhang, Ying, Wang, Dong, Tan, Li-Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600687/
https://www.ncbi.nlm.nih.gov/pubmed/34794508
http://dx.doi.org/10.1186/s41065-021-00211-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600687/
https://www.ncbi.nlm.nih.gov/pubmed/34794508
http://dx.doi.org/10.1186/s41065-021-00211-y

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