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2662 : FOXE3 mutations correlations between mutation types, inheritance pattern, and phenotype severity

Researchers

Presenter

  • J. Plaisanci

Principal Investigators

  • N. Ragge

  • H. Dollfus

  • J. Kaplan

  • D. Lehalle

  • C. Francannet

  • G. Morin

  • H. Colineaux

  • P. Calvas

  • N. Chassaing

Medical Centers

  • Génétique Médicale, Hôpital Purpan, Toulouse, France

  • INSERM U1056, Université Toulouse Iii, Toulouse, France

  • Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, United Kingdom

  • West Midlands Regional Genetics Laboratories, Birmingham Womens NHS Foundation Trust, Birmingham, United Kingdom

  • Cargo‐ Filière Sensgene, Hôpitaux Universitaires De Strasbourg, Strasbourg, France

  • Génétique Ophtalmologique, Inserm U1163, Paris, France

  • Centre De Génétique Et Centre De Référence Anomalies Du Développement Et Syndromes Malformatifs, Hôpital D'enfants, Dijon, France

  • Service De Génétique Médicale, Chu Estaing‐, Clermont‐Ferrand, France

  • Service De Génétique, Hôpital Nord D'amiens, Amiens, France

  • University Hospital of Toulouse, Department of Epidemiology, Health Economics and Public Health, Toulouse, France

Locations

  • France

  • United Kingdom

Companies

  • N/A

Study Components

Therapeutic Area

  • N/A

Disease

  • N/A

Biomarkers

  • N/A

Drug/Treatment

  • N/A

Outcome

  • N/A

Study Design

  • N/A

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • N/A

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