Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men

[1] Reijo R(1995)Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene Nat Genet 10 383-393

[2] Lee TY(2002)Genetic dissection of mammalian fertility pathway Nat Med 8 S41-S49

[3] Salo P(2003)Azoospermia in patients heterozygous for a mutation in SYCP3 Lancet 362 1714-1719

[4] Alagappan R(2006)Protamines and male infertility Hum Reprod Update 12 417-435

[5] Brown LG(2007)Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia Am J Hum Genet 81 813-820

[6] Rosenberg M(2007)Homozygous mutation of AURKC yields large-headed polyploidy spermatozoa and causes male infertility Nat Genet 39 661-665

[7] Matzuk MM(2006)Non-invasive genetic diagnosis of male infertility using spermatozoa RNA: KLHL10 mutations in oligozoospermic patients impair homodimerization Hum Mol Genet 15 3411-3419

[8] Lamb DJ(2001)Study of microdeletions in the Y chromosome of infertile men with idiopathic oligo- or azoospermia J Assist Reprod Genet 18 612-616

[9] Miyamoto T(2010)BCL2 Ala43Thr is a functional variant associated with protection against azoospermia in a Han-Chinese population Biol Reprod 83 656-662

[10] Hasuike S(2010)The role of endothelial nitric oxide synthase (eNOS) T-786C, G894T, and 4a/b gene polymorphisms in the risk of idiopathic male infertility Mol Reprod Dev 77 720-727

[1] Reijo R(1995)Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene Nat Genet 10 383-393

[2] Lee TY(2002)Genetic dissection of mammalian fertility pathway Nat Med 8 S41-S49

[3] Salo P(2003)Azoospermia in patients heterozygous for a mutation in SYCP3 Lancet 362 1714-1719

[4] Alagappan R(2006)Protamines and male infertility Hum Reprod Update 12 417-435

[5] Brown LG(2007)Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia Am J Hum Genet 81 813-820

[6] Rosenberg M(2007)Homozygous mutation of AURKC yields large-headed polyploidy spermatozoa and causes male infertility Nat Genet 39 661-665

[7] Matzuk MM(2006)Non-invasive genetic diagnosis of male infertility using spermatozoa RNA: KLHL10 mutations in oligozoospermic patients impair homodimerization Hum Mol Genet 15 3411-3419

[8] Lamb DJ(2001)Study of microdeletions in the Y chromosome of infertile men with idiopathic oligo- or azoospermia J Assist Reprod Genet 18 612-616

[9] Miyamoto T(2010)BCL2 Ala43Thr is a functional variant associated with protection against azoospermia in a Han-Chinese population Biol Reprod 83 656-662

[10] Hasuike S(2010)The role of endothelial nitric oxide synthase (eNOS) T-786C, G894T, and 4a/b gene polymorphisms in the risk of idiopathic male infertility Mol Reprod Dev 77 720-727