Novel Compound Heterozygous Mutation in a Sporadic Family Associated with Spermatogenetic Failure
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References
1.
Krausz C, Riera-Escamilla A
. Genetics of male infertility. Nat Rev Urol. 2018; 15(6):369-384.
DOI: 10.1038/s41585-018-0003-3.
View
2.
Libby B, Reinholdt L, Schimenti J
. Positional cloning and characterization of Mei1, a vertebrate-specific gene required for normal meiotic chromosome synapsis in mice. Proc Natl Acad Sci U S A. 2003; 100(26):15706-11.
PMC: 307632.
DOI: 10.1073/pnas.2432067100.
View
3.
Sato H, Miyamoto T, Yogev L, Namiki M, Koh E, Hayashi H
. Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest. J Hum Genet. 2006; 51(6):533-540.
DOI: 10.1007/s10038-006-0394-5.
View
4.
Libby B, De La Fuente R, OBrien M, Wigglesworth K, Cobb J, Inselman A
. The mouse meiotic mutation mei1 disrupts chromosome synapsis with sexually dimorphic consequences for meiotic progression. Dev Biol. 2002; 242(2):174-87.
DOI: 10.1006/dbio.2001.0535.
View
5.
Li B, Wu W, Luo H, Liu Z, Liu H, Li Q
. Molecular characterization and epigenetic regulation of Mei1 in cattle and cattle-yak. Gene. 2015; 573(1):50-6.
DOI: 10.1016/j.gene.2015.07.021.
View