Two Different Sequencing Platforms Identified an Additional Phenotype Caused by a HOXA2 Variant in a Family with Mixed Hearing Loss and Middle Ear Anomaly without Microtia
Two Different Sequencing Platforms Identified an Additional Phenotype Caused by a HOXA2 Variant in a Family with Mixed Hearing Loss and Middle Ear Anomaly without Microtia
复制标题
两个不同的测序平台在一个患有混合性听力损失和中耳异常（无小耳症）的家庭中鉴定出由 HOXA2 变异引起的额外表型
DOI：
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发表时间：
2019
期刊：
影响因子：
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通讯作者：
Shin-ichi Usami
中科院分区：
文献类型：
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作者：
Yoshihiro Noguchi;Shin-ya Nishio;Shin-ichi Usami
