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Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest
PURPOSE: To investigate whether defects in human PRDM9, CDK2 and PSMC3IP are associated with azoospermia Mutational analysis was performed in Japanese patients with azoospermia caused by meiotic arrest. METHODS: Mutational screening of the coding regions of human PRDM9, CDK2 and PSMC3IP was done by...
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| Hoofdauteurs: | , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Springer US
2008
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2593767/ https://ncbi.nlm.nih.gov/pubmed/18941885 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-008-9270-x |
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