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Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family
Ma, Yalin; Xiao, Yun; Zhang, Fengguo; Han, Yuechen; Li, Jianfeng; Xu, Lei; Bai, Xiaohui; Wang, Haibo
刊名INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
2016
卷号83期号:4页码:179-185
关键词Deafness Autosomal recessive inheritance MYO7A gene Mutation
DOI10.1016/j.ijporl.2016.01.001
URL标识查看原文
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/4693357
专题山东大学
作者单位Shandong Univ, Dept Otorhinolaryngol Head & Nec
推荐引用方式
GB/T 7714
Ma, Yalin,Xiao, Yun,Zhang, Fengguo,et al. Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family[J]. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY,2016,83(4):179-185.
APA Ma, Yalin.,Xiao, Yun.,Zhang, Fengguo.,Han, Yuechen.,Li, Jianfeng.,...&Wang, Haibo.(2016).Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family.INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY,83(4),179-185.
MLA Ma, Yalin,et al."Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family".INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY 83.4(2016):179-185.
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