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Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella.
Martinez, Guillaume; Kherraf, Zine-Eddine; Zouari, Raoudha; Fourati Ben Mustapha, Selima; Saut, Antoine; Pernet-Gallay, Karin; Bertrand, Anne; Bidart, Marie; Hograindleur, Jean Pascal; Amiri-Yekta, Amir; Kharouf, Mahmoud; Karaouzène, Thomas; Thierry-Mieg, Nicolas; Dacheux-Deschamps, Denis; Satre, Véronique; Bonhivers, Mélanie; Touré, Aminata; Arnoult, Christophe; Ray, Pierre F; Coutton, Charles.
Afiliação
  • Martinez G; University Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Institute for Advanced Biosciences, Team Genetics Epigenetics and Therapies of Infertility, Grenoble, France.
  • Kherraf ZE; CHU Grenoble Alpes, UM de Génétique Chromosomique, Grenoble, France.
  • Zouari R; University Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Institute for Advanced Biosciences, Team Genetics Epigenetics and Therapies of Infertility, Grenoble, France.
  • Fourati Ben Mustapha S; CHU de Grenoble, UM GI-DPI, Grenoble, France.
  • Saut A; Clinique des Jasmins, 23, Av. Louis BRAILLE 1002 Belvedere, Tunis, Tunisia.
  • Pernet-Gallay K; Clinique des Jasmins, 23, Av. Louis BRAILLE 1002 Belvedere, Tunis, Tunisia.
  • Bertrand A; University Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Institute for Advanced Biosciences, Team Genetics Epigenetics and Therapies of Infertility, Grenoble, France.
  • Bidart M; CHU Grenoble Alpes, UM de Génétique Chromosomique, Grenoble, France.
  • Hograindleur JP; Grenoble Neuroscience Institute, INSERM 1216, Grenoble, France.
  • Amiri-Yekta A; Grenoble Neuroscience Institute, INSERM 1216, Grenoble, France.
  • Kharouf M; CHU Grenoble Alpes, UM de Biochimie Génétique et Moléculaire, Grenoble, France.
  • Karaouzène T; University Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Institute for Advanced Biosciences, Team Genetics Epigenetics and Therapies of Infertility, Grenoble, France.
  • Thierry-Mieg N; University Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Institute for Advanced Biosciences, Team Genetics Epigenetics and Therapies of Infertility, Grenoble, France.
  • Dacheux-Deschamps D; CHU Grenoble Alpes, UM de Biochimie Génétique et Moléculaire, Grenoble, France.
  • Satre V; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
  • Bonhivers M; Clinique des Jasmins, 23, Av. Louis BRAILLE 1002 Belvedere, Tunis, Tunisia.
  • Touré A; University Grenoble Alpes, INSERM U1209, CNRS UMR 5309, Institute for Advanced Biosciences, Team Genetics Epigenetics and Therapies of Infertility, Grenoble, France.
  • Arnoult C; University Grenoble Alpes/CNRS, TIMC-IMAG, Grenoble, France.
  • Ray PF; University Grenoble Alpes/CNRS, TIMC-IMAG, Grenoble, France.
  • Coutton C; Université de Bordeaux, Microbiologie Fondamentale et Pathogénicité, CNRS UMR, Bordeaux, France.
Hum Reprod ; 33(10): 1973-1984, 2018 10 01.
Article em En | MEDLINE | ID: mdl-30137358
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cauda do Espermatozoide / Teratozoospermia Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cauda do Espermatozoide / Teratozoospermia Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article