Common genetic variation in KATNAL1 non‐coding regions is involved in the susceptibility to severe phenotypes of male infertility
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DOI: 10.1111/andr.13221
Abstract: Previous studies in animal models evidenced that genetic mutations of KATNAL1, resulting in dysfunction of its encoded protein, lead to male infertility through disruption of microtubule remodelling and premature germ cell exfoliation. Subsequent studies in… read more here.
Keywords: genetic variation; common genetic; variation katnal1; infertility ... See more keywords