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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Detalhes bibliográficos
Publicado no:Am J Hum Genet
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2019
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Article
Acesso em linha: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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