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Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment

URI: https://hdl.handle.net/10550/123550
DOI: https://doi.org/10.1016/j.fertnstert.2020.02.115
2020
Cerván-Martín, Miriam
Rivera-Egea, Rocío
Rocío Rivera-Egea
Garrido Puchalt, Nicolás
Luján Marco, Satur
Romeu, Gema
Quintana, Fernando
impotència sexual, home, aparell genitourinari malalties

To evaluate whether SOHLH2 intronic variation contributes to the genetic predisposition to male infertility traits, including severe oligospermia (SO) and different nonobstructive azoospermia (NOA) clinical phenotypes.

32 - Ciències Médiques
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Cerván-Martín, Miriam
;
Rivera-Egea, Rocío
;
Rocío Rivera-Egea
;
Garrido Puchalt, Nicolás
;
Luján Marco, Satur
;
Romeu, Gema
;
Quintana, Fernando