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Severe oligozoospermia (SO) is an important cause of male infertility. Its etiology and pathogenesis are associated with genetic abnormalities; however, the genetic causes of the majority of idiopathic human SO remain unclear. Here, we report a homozygous splice‐site mutation in M1AP (meiosis 1 associated protein; NM_138804, c.1435‐1G>A) observed in a patient with SO from a consanguineous Han Chinese...
The cover image is based on the Short Report An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family by Chaofeng Tu and Ying Wang et al., https://doi.org/10.1111/cge.13712.
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