{Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum}
Abstract
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility
Abstract
Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility
Abstract
The genetic architecture of morphological abnormalities of the sperm tail
Abstract
Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum
Abstract
Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse
Abstract
Correction to: 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
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
Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa
Abstract
Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility
Abstract