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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Main Authors: Miyamoto, Toshinobu, Koh, Eitetsu, Sakugawa, Naoko, Sato, Hisashi, Hayashi, Hiroaki, Namiki, Mikio, Sengoku, Kazuo
Formato: Artigo
Idioma:Inglês
Publicado: Springer US 2008
Assuntos:
Genetics
Acceso en liña: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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