机译:SLC12A5 SLC12A5 SLC12A5中的DE Novo畸形突变在复合杂合子患者中发现,具有迁移焦点癫痫发作的癫痫患者
Department of Child Neurology National Center HospitalNational Center of Neurology and;
Department of Pediatrics School of MedicineFukuoka UniversityFukuoka Japan;
Department of Child Neurology National Center HospitalNational Center of Neurology and;
Department of Child Neurology National Center HospitalNational Center of Neurology and;
Department of Pediatrics School of MedicineFukuoka UniversityFukuoka Japan;
channel; epileptic encephalopathy; gene test; K + –Cl ? cotransporter; next generation sequencing; NGS; SLC12A5;
机译:SLC12A5 SLC12A5 SLC12A5中的DE Novo畸形突变在复合杂合子患者中发现,具有迁移焦点癫痫发作的癫痫患者
机译:婴儿癫痫发作中 SLC12A5 i>的突变,伴有局灶性癫痫发作
机译:在迁移局灶性发作和严重发育迟缓的等位基因突变SLC12A5神经元受损KCC2功能
机译:癫痫患者遥控监测和癫痫发作警告系统框架的设计
机译:神经发育障碍中的Novo畸形突变
机译:婴儿癫痫发作伴有局灶性癫痫发作的SLC12A5突变
机译:婴儿癫痫发作伴有局灶性癫痫发作的SLC12A5突变