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Novel Variants in DNAH9 Lead to Nonsyndromic Severe Asthenozoospermia

2021-02-12

Abstract excerpt

<title>Abstract</title> <p><bold>Background </bold>Asthenozoospermia is one of the most common causes of male infertility, and its genetic etiology is poorly understood. DNAH9 is a core component of outer dynein arms in cilia and flagellum. It was reported that variants of <italic>DNAH9 </italic>(OMIM: 603330) might cause primary ciliary dyskinesia (PCD). However, variants in <italic>DNAH9</italic> lead to nonsyn...

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Literature Corpus work
d3ea0e7c-d5fe-5730-9832-a701249ed3a5
DOI
10.21203/rs.3.rs-197024/v1
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Novel Variants in DNAH9 Lead to Nonsyndromic Severe AsthenozoospermiaDOI 10.21203/rs.3.rs-197024/v1
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