Association of the c.‐9C>T and c.368A>G transitions in H2BFWT gene with male infertility in an Iranian population

Summary The H2BFWT (H2B family, member W, testis specific) gene is a testis‐specific histone which is involved in the spermatogenesis process. This study aimed to investigate the association of H2BFWT gene c.‐9C>T and c.368A>G polymorphisms with male infertility in an Iranian population. The 2...

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Veröffentlicht in:	Andrologia 2018-02, Vol.50 (1), p.e12805-n/a
Hauptverfasser:	Rafatmanesh, A., Nikzad, H., Ebrahimi, A., Karimian, M., Zamani, T.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alleles genetic polymorphism H2BFWT gene Infertility male infertility Oligozoospermia PCR‐RFLP Polymerase chain reaction Restriction fragment length polymorphism Risk factors Spermatogenesis
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