论文部分内容阅读
A novel de novo mutation of ACTG1 in two sporadic non-syndromic hearing loss cases
【机 构】
：
ChinesePLAInstituteofOtolaryngology,BeijingCentreforPhysicalandChemicalAnalysis
【出 处】
：
中国科学：生命科学英文版
【发表日期】
：
2018年6期
【基金项目】
：
supported by the National Natural Science Foundation of China（81530032）, the National Key Basic Research Program of China（2014CB943001）
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