一个MYO15A基因新的复合杂合位点突变导致先天性聋病例分析
亓文晶;王雅宁;于萌萌;张楠;张巍;古林涛;
1:山东第一医科大学(山东省医学科学院)
2:山东第一医科大学第一附属医院(山东省千佛山医院)耳鼻喉科
3:山东省济宁市邹城市兖矿新里程总医院
4:广州嘉检医学检测有限公司
摘要关键词基金项目(Foundation):作者参考文献1 李靖宇，李云龙.非综合征型遗传性耳聋相关致病基因的研究进展[J].医药前沿，2019,9(11):10-11.
2 赵亚茹，宋亮亮.新生儿听力筛查与耳聋的基因诊断[J].实用儿科临床杂志，2010,25(11):790-791.
3 孙莉莉，张莉，张东红.小儿非综合征型耳聋 59例基因突变筛查分析[J].中国实用儿科杂志，2014,29(2):133-136.
4 宋亮亮，赵亚茹.GJB2基因及其诊断筛查技术研究进展[J].国际儿科学杂志，2010,37(5):545-547.
5 任晓菲，朱姝，朱宝生，等.MYO15A基因突变在非综合征型聋中的研究进展[J].听力学及言语疾病杂志，2017,25(4):436-440.
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