• 江南大学附属儿童医院 神经内科(无锡 214000);
孙明霞, Email: sdjnsmxscj@163.com
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Citation: 周逸能, 孙明霞, 华颖, 陈李兰. MYT1L基因变异所致常染色体显性精神发育迟滞39型一例临床与遗传学分析. Journal of Epilepsy, 2025, 11(3): 266-270. doi: 10.7507/2096-0247.202502014 Copy

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