Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella
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A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility
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CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report
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Deletions on mouse Yq lead to upregulation of multiple X- and Y-linked transcripts in spermatids
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The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility
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Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility
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Genetics of teratozoospermia: Back to the head
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Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility
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Biallelic variants in <i>MAATS1</i> encoding CFAP91, a calmodulin-associated and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility
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TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella
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