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Shaobin Lin

Boston Children's Hospital

4

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37

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Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype.

2020 Journal of Human Genetics
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CCDC9 is identified as a novel candidate gene of severe asthenozoospermia

2019 Systems Biology in Reproductive Medicine
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DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella

2019 Annals of Human Genetics
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EIF4G1 is a novel candidate gene associated with severe asthenozoospermia

2019 Molecular Genetics & Genomic Medicine
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