Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human
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Published:2018-02-15
Issue:1
Volume:9
Page:
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ISSN:2041-1723
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Container-title:Nature Communications
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language:en
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Short-container-title:Nat Commun
Author:
Coutton Charles, Vargas Alexandra S.ORCID, Amiri-Yekta AmirORCID, Kherraf Zine-Eddine, Ben Mustapha Selima Fourati, Le Tanno Pauline, Wambergue-Legrand Clémentine, Karaouzène Thomas, Martinez Guillaume, Crouzy Serge, Daneshipour Abbas, Hosseini Seyedeh Hanieh, Mitchell Valérie, Halouani Lazhar, Marrakchi Ouafi, Makni Mounir, Latrous Habib, Kharouf Mahmoud, Deleuze Jean-François, Boland Anne, Hennebicq Sylviane, Satre Véronique, Jouk Pierre-Simon, Thierry-Mieg Nicolas, Conne Beatrice, Dacheux Denis, Landrein Nicolas, Schmitt Alain, Stouvenel Laurence, Lorès Patrick, El Khouri Elma, Bottari Serge P., Fauré Julien, Wolf Jean-Philippe, Pernet-Gallay Karin, Escoffier Jessica, Gourabi Hamid, Robinson Derrick R., Nef Serge, Dulioust Emmanuel, Zouari Raoudha, Bonhivers MélanieORCID, Touré Aminata, Arnoult Christophe, Ray Pierre F.ORCID
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Reference65 articles.
1. Coutton, C., Fissore, R. A., Palermo, G. D., Stouffs, K. & Touré, A. Male infertility: genetics, mechanism, and therapies. Biomed. Res. Int. 2016, 7372362 (2016). 2. Coutton, C., Escoffier, J., Martinez, G., Arnoult, C. & Ray, P. F. Teratozoospermia: spotlight on the main genetic actors in the human. Hum. Reprod. Update 21, 455–485 (2015). 3. Ray, P. F. et al. Genetic abnormalities leading to qualitative defects of sperm morphology or function. Clin. Genet. 91, 217–232 (2017). 4. Kherraf, Z.-E. et al. SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes. EMBO Mol. Med. 9, 1132–1149 (2017). 5. Ben Khelifa, M. et al. Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella. Am. J. Hum. Genet. 94, 95–104 (2014).
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