一个常染色体显性遗传非综合征型聋家系MYO6基因新致病性变异
Identification of a Novel MYO6 Mutation Associated with Autosomal Dominant Non-syndromic Hearing Loss in a Chinese Family by Whole-exome Sequencing
田涛;鲁雅洁;姚俊;曹新;魏钦俊;李琦;
1:南京医科大学附属儿童医院耳鼻咽喉科
2:南京医科大学基础医学院生物技术系
3:南京大学医学院附属儿童医院耳鼻咽喉科
摘要关键词基金项目(Foundation):作者参考文献1 Sommen M,Wuyts W,Van Camp G,et al.Molecular diagnostics for hereditary hearing loss in children [J].Expert Rev Mol Diagn,2017,17:751.
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