非综合征型聋患者及家庭成员耳聋基因MYO15A检测及其产前诊断意义
MYO15A Gene Mutation Analysis for Two Nonsyndromic Sensorineural Hearing Loss Families and Their Prenatal Diagnosis
柴福;赵海亮;李胜;林晋业;魏建芳;邱书奇;
1:深圳市龙岗区耳鼻咽喉医院
2:深圳市耳鼻咽喉研究所
3:深圳市耳鼻咽喉重点实验室
摘要关键词基金项目(Foundation):作者参考文献1 Lazar C,Popp R,Trifa A,et al.Prevalence of the c.35delG and p.W24Xmutation in the GJB2gene in patients with nonsyndromic hearing loss fromNorth-WestRomania[J].Int J Pediatr Otorhinolaryngol,2010,74:351.
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