Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure

Author:

Riera-Escamilla Antoni,Vockel Matthias,Nagirnaja Liina,Xavier Miguel J.,Carbonell Albert,Moreno-Mendoza Daniel,Pybus Marc,Farnetani Ginevra,Rosta Viktoria,Cioppi Francesca,Friedrich Corinna,Oud Manon S.,van der Heijden Godfried W.,Soave Armin,Diemer Thorsten,Ars Elisabet,Sánchez-Curbelo Josvany,Kliesch Sabine,O’Bryan Moira K.,Ruiz-Castañe Eduard,Azorín Fernando,Veltman Joris A.,Aston Kenneth I.,Conrad Donald F.,Tüttelmann Frank,Krausz Csilla

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference60 articles.

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3. A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene–disease relationships;Houston;Hum. Reprod.,2021

4. Genetic factors of non-obstructive azoospermia: consequences on patients’ and offspring Health;Krausz;J. Clin. Med.,2021

5. The mouse X chromosome is enriched for multicopy testis genes showing postmeiotic expression;Mueller;Nat. Genet.,2008

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