Boudjelida KamelService Ophtalmologie Centre Hospitalier universitaire de Blida关注立即认领分享关注立即认领分享基本信息浏览量:1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Diversity Of The Genes Implicated In Algerian Patients Affected By Usher SyndromeSamia Abdi,Amel Bahloul,Asma Behlouli,Jean-Pierre Hardelin,Mohamed Makrelouf,Kamel Boudjelida,Malek Louha, Ahmed Cheknene, Rachid Belouni,Yahia Rous, Zahida Merad, Djamel Selmane,PLOS ONE(2016)引用21浏览0WOS引用210EPS8 , encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafnessAsma Behlouli,Crystel Bonnet,Samia Abdi,Aïcha Bouaita,Andrea Lelli,Jean-Pierre Hardelin,Cataldo Schietroma,Yahia Rous,Malek Louha,Ahmed Cheknane,Hayet Lebdi,Kamel Boudjelida,Orphanet journal of rare diseases(2014)引用62浏览0WOS引用620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