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.
Abstract
Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.
Abstract
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility.
Abstract
Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.
Abstract