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HARVARD Citation
Xu, X. et al. (2018). A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole‐exome sequencing. Clinical genetics. 93 (2), pp. 345-349. [Online].
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Xu, X. et al. (2018). A familial study of twins with severe asthenozoospermia identified a homozygous SPAG17 mutation by whole‐exome sequencing. Clinical genetics. 93 (2), pp. 345-349. [Online].