Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility

In humans, structural or functional defects of the sperm flagellum induce asthenozoospermia, which accounts for the main sperm defect encountered in infertile men. Herein we focused on morphological abnormalities of the sperm flagellum (MMAF), a phenotype also termed “short tails,” which constitutes...

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Veröffentlicht in:Am J Hum Genet
Hauptverfasser: Lorès, Patrick, Dacheux, Denis, Kherraf, Zine-Eddine, Nsota Mbango, Jean-Fabrice, Coutton, Charles, Stouvenel, Laurence, Ialy-Radio, Come, Amiri-Yekta, Amir, Whitfield, Marjorie, Schmitt, Alain, Cazin, Caroline, Givelet, Maëlle, Ferreux, Lucile, Fourati Ben Mustapha, Selima, Halouani, Lazhar, Marrakchi, Ouafi, Daneshipour, Abbas, El Khouri, Elma, Do Cruzeiro, Marcio, Favier, Maryline, Guillonneau, François, Chaudhry, Marhaba, Sakheli, Zeinab, Wolf, Jean-Philippe, Patrat, Catherine, Gacon, Gérard, Savinov, Sergey N., Hosseini, Seyedeh Hanieh, Robinson, Derrick R., Zouari, Raoudha, Ziyyat, Ahmed, Arnoult, Christophe, Dulioust, Emmanuel, Bonhivers, Mélanie, Ray, Pierre F., Touré, Aminata
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier 2019
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Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6904810/
https://ncbi.nlm.nih.gov/pubmed/31735292
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2019.10.007
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