Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human.
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Homozygous missense mutation L673P in Adenylate Kinase 7 (AK7) leads to primary male infertility and Multiple Morphological Anomalies of the Flagella but not to Primary Ciliary Dyskinesia.
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Genetic causes of male infertility: snapshot on morphological abnormalities of the sperm flagellum.
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Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice.
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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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Slc26a3 deficiency is associated with epididymis dysplasia and impaired sperm fertilization potential in the mouse.
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Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.
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CFAP70 mutations lead to male infertility due to severe astheno-teratozoospermia. A case report.
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Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.
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