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Whole-exome sequencing identifies two novel MARVELD2 frame-shift mutations as a cause of autosomal r
[会议论文] 作者：,Tang Ning,Li Wugao,Li Zhetao,Luo Shiqiang,Li Jingwen,Cai Ren,Tang Xiangrong,Yang Yan,Wang Lin,Zeng Dingyuan,
来源：第十五次中国中西医结合耳鼻咽喉科专业委员会年会 年份：2016
Background The genetic heterogeneity of hearing loss makes genetic diagnosis expensive and time consuming using available methods....
Identification and Clinical Implications of Novel MY015A Mutations in a Non-consanguineous Chinese F
[会议论文] 作者：Tizhen,Li Zhetao,Li Wugao,Tang Ning,Li Jingwen,Cai Ren,Tang Xiangrong,Yang Yan,Zheng Pei,Wang Lin,Zeng Dingyuan,
来源：第十五次中国中西医结合耳鼻咽喉科专业委员会年会 年份：2016
Autosomal recessive nonsyndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder, generally manifested with prelingual hearing l...
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