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CJCP
2022 24 (5):
585-590
ISSN: 1008-8830 CN: 43-1301/R
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Clinical phenotype and genetic features of 16p11.2 microdeletion-related epilepsy in children |
LAI Chong-Yuan, CHEN Rui-Hua, ZHONG Chun-Lan, JI Ming-Ming, LI Bing-Fei |
Center of Epilepsy Diagnosis and Treatment, Department of Pediatric Neurology, Ganzhou Maternal and Child Health Care Hospital, Ganzhou, Jiangxi 341000, China (Chen R-H, Email: crh16899@sina.cn) |
Received: 2021-11-19 Revised: null Online: null |
Supporting info
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