Articles with "mutations ttc29" as a keyword



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Novel biallelic mutations in TTC29 cause asthenoteratospermia and male infertility

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Published in 2022 at "Molecular Genetics & Genomic Medicine"

DOI: 10.1002/mgg3.2078

Abstract: Multiple morphological abnormalities of the sperm flagella (MMAF), which is characterized as asthenoteratospermia involving absent, short, bent, coiled, and/or irregularā€caliber flagella, is a rare recessive inherited disorder associated with male infertility. To date, genetic causes… read more here.

Keywords: novel biallelic; mutations ttc29; biallelic mutations; asthenoteratospermia ... See more keywords