Novel variant in CHRNA4 with benign childhood epilepsy with centrotemporal spikes and contribution to precise medicine.
Xiao NengXiao MaoChen YuanluLi QinyanShu LiSong ZhanyiPublished in: Molecular genetics & genomic medicine (2020)
This is the first study on CHRNA4 variant in BECTS, which widened the genetic spectrum of BECTS and contributed to precise medicine in BECTS.