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Identification of a novel deletion mutation in DPY19L2 from an infertile patient with globozoospermia: a case report.
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- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00495-1
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Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility.
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- Asian Journal of Andrology, 2022, v. 24, n. 1, p. 67, doi. 10.4103/aja.aja_56_21
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- Article