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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| Автори: | , , , , , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
BMC
2021-11-01
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| Серія: | Hereditas |
| Предмети: | |
| Онлайн доступ: | https://doi.org/10.1186/s41065-021-00211-y |
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