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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Vydáno v:Am J Hum Genet
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Elsevier 2019
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On-line přístup: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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