Identifies a GABRA4 variant contributing to developmental delay and epilepsy, highlighting genetic influences on neurological disorders.
The authors declare no conflicts of interest. The data that support the findings of this study are available on request from the corresponding author. The data are not publicly available due to privacy or ethical restrictions. Table S1: Candidate variants identified by trio exome sequencing. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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