Archives of Biological Sciences · 2010 · 16 citations · 21 references
MedicineGeneticsMolecular GeneticsFertilityHuman GeneticsInfertilityGenetic Basis Of InfertilityGenetic DisordersInfertility EpidemiologyMale InfertilityReproductive RiskGene DeletionGenetic Markers Of FertilityHereditary Infertility RiskMale Infertility Epidemiology
The aim of the study was to investigate the association between the GSTM1 and GSTT1 gene deletion and MTHFR C677T mutation and male infertility. The study has encompassed 52 infertile and 56 fertile males. Genotype distributions of GSTM1 and GSTT1 gene deletions and the MTHFR C677T mutation did not differ significantly among the analyzed groups, however, a difference in distribution of certain genotype combinations was observed. The obtained results indicate that carriers of double GSTM1/GSTT1 deletion and the MTHFR 677CC genotype are at higher risk of infertility than carriers of any other combination of genotypes (OR 3.5, 95%CI 0.68-18.30). .
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Simonetta Friso, Sang‐Woon Choi, Domenico Girelli et al. · Proceedings of the National Academy of Sciences · 2002 · 931 citations
Genetics of human male infertility.
J Poongothai, TS Gopenath, S Manonayaki · PubMed · 2009 · 345 citations
Medicine, Genetics, Infertility +12