The genetic architecture of morphological abnormalities of the sperm tail.
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A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.
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Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.
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The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility.
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Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.
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