Dagmar RaskovaCentre for Medical Genetics and Reproductive Medicine Gennet, Czech Republic关注立即认领分享关注立即认领分享基本信息浏览量:0职业迁徙个人简介暂无内容研究兴趣论文共 2 篇作者统计合作学者相似作者按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选时间引用量主题期刊级别合作者合作机构Spectrum And Frequencies Of Non Gjb2 Gene Mutations In Czech Patients With Early Non-Syndromic Hearing Loss Detected By Gene Panel Ngs And Whole-Exome SequencingDana Safka Brozkova, Simona Poisson Marková,Anna Uhrová Mészárosová,Jan Jencik,Zdenek Cada,Jana Lastuvkova,Dagmar Raskova,Pavel SeemanCLINICAL GENETICS(2020)引用20浏览0WOS引用200Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC geneZdeněk Čada,Dana Šafka Brožková,Zuzana Balatková,Pavlína Plevová,Dagmar Rašková,Jana Laštůvková,Rudolf Černý, Veronika Bandúrová,Vladimír Koucký,Silvie Hrubá,Martin Komarc,Ján Jenčík,Eur Arch Otorhinolaryngol(2019)引用14浏览0WOS引用140作者统计合作学者合作机构D-Core合作者学生导师暂无相似学者,你可以通过学者研究领域进行搜索筛选数据免责声明页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn