Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives
Author:
Funder
Eesti Teadusagentuur
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-020-02112-y.pdf
Reference150 articles.
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3. Arafat M et al (2017) Mutation in TDRD9 causes non-obstructive azoospermia in infertile men. J Med Genet 54:633–639. https://doi.org/10.1136/jmedgenet-2017-104514
4. Ayhan O, Balkan M, Guven A, Hazan R, Atar M, Tok A, Tolun A (2014) Truncating mutations in TAF4B and ZMYND15 causing recessive azoospermia. J Med Genet 51:239–244. https://doi.org/10.1136/jmedgenet-2013-102102
5. Ballow D, Meistrich ML, Matzuk M, Rajkovic A (2006) Sohlh1 is essential for spermatogonial differentiation. Dev Biol 294:161–167. https://doi.org/10.1016/j.ydbio.2006.02.027
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