| Literature DB >> 33224017 |
Ozlem Gorukmez1, Orhan Gorukmez1.
Abstract
Male infertility is multifactorial and presents with heterogeneous phenotypic features. Genetic factors are responsible for up to 15% of the male infertility cases. Loss of the Cstf2t gene in male mice results in infertility. No disease-associated mutations have been described for this gene in infertile men. Here, we report a patient diagnosed with infertility in whom a homozygous nonsense mutation in the CSTF2T gene was detected by clinical exome sequencing. This case is the first description of an infertile patient who has a homozygous CSTF2T mutation.Entities:
Keywords: CSTF2T; Clinical exome sequencing; Infertility; Novel mutation
Year: 2020 PMID: 33224017 PMCID: PMC7675224 DOI: 10.1159/000509686
Source DB: PubMed Journal: Mol Syndromol ISSN: 1661-8769