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Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella

dc.rights.licenseopenen_US
dc.contributor.authorMARTINEZ, Guillaume
dc.contributor.authorKHERRAF, Zine-Eddine
dc.contributor.authorZOUARI, Raoudha
dc.contributor.authorFOURATI BEN MUSTAPHA, Selima
dc.contributor.authorSAUT, Antoine
dc.contributor.authorPERNET-GALLAY, Karin
hal.structure.identifierUniversité de Bordeaux [UB]
dc.contributor.authorBERTRAND, Anne
dc.contributor.authorBIDART, Marie
dc.contributor.authorHOGRAINDLEUR, Jean Pascal
dc.contributor.authorAMIRI-YEKTA, Amir
dc.contributor.authorKHAROUF, Mahmoud
dc.contributor.authorKARAOUZÈNE, Thomas
dc.contributor.authorTHIERRY-MIEG, Nicolas
dc.contributor.authorDACHEUX-DESCHAMPS, Denis
dc.contributor.authorSATRE, Véronique
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBONHIVERS, Melanie
dc.contributor.authorTOURÉ, Aminata
dc.contributor.authorARNOULT, Christophe
dc.contributor.authorRAY, Pierre
dc.contributor.authorCOUTTON, Charles
dc.date.accessioned2023-06-21T13:55:54Z
dc.date.available2023-06-21T13:55:54Z
dc.date.issued2018-10-01
dc.identifier.issn0268-1161en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/182749
dc.language.isoENen_US
dc.title.enWhole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/humrep/dey264en_US
dc.subject.halSciences du Vivant [q-bio]/Bio-Informatique, Biologie Systémique [q-bio.QM]en_US
bordeaux.journalHuman Reproductionen_US
bordeaux.page1973 - 1984en_US
bordeaux.volume33en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue10en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-01877993
hal.version1
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
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