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   <subfield code="a">Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Toshinobu Miyamoto, Akira Tsujimura, Yasushi Miyagawa, Eitetsu Koh, Mikio Namiki, Michiharu Horikawa, Yasuaki Saijo, Kazuo Sengoku]</subfield>
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   <subfield code="a">Purpose: To investigate the association between the UBR2 gene and the risk of azoospermia caused by meiotic arrest. Methods: Mutational analysis of the UBR2 gene was performed using DNA from 30 patients with azoospermia by meiotic arrest to 80 normal controls. Results: The genotypic and allelic frequencies of c.1,066A&gt;T variant were significantly higher in patient than control groups (p &lt; 0.001). Conclusion: The c.1,066A&gt;T variant in the UBR2 gene is associated with increased susceptibility to azoospermia caused by meiotic arrest.</subfield>
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