This study was supported by grants from the Région des Pays de la Loire (project “EryCan”); the ANR (PRTS 2015 “GenRED” and AAPG 2020 “SplicHypoxia”); the labex GR-Ex, reference ANR-11-LABX-0051; Fonds Européen de Développement Régional (FEDER) Bourgogne Franche Comté; the VHL Alliance USA, the VHL France; the Génavie association and the Fondation Maladies Rares (FMR).

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This study was supported by grants from the Région des Pays de la Loire (project “EryCan”); the ANR (PRTS 2015 “GenRED” and AAPG 2020 “SplicHypoxia”); the labex GR-Ex, reference ANR-11-LABX-0051; Fonds Européen de Développement Régional (FEDER) Bourgogne Franche Comté; the VHL Alliance USA, the VHL France; the Génavie association and the Fondation Maladies Rares (FMR).

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Issue DateTitleAuthor(s)TypeAccess
11-Nov-2023Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosisDelamare, Marine; Le Roy, Amandine; Pacault, Mathilde; Schmitt, Loïc; Garrec, Céline; Maaziz, Nada; Myllykoski, Matti; Rimbert, Antoine; Karaghiannis, Valéna; Aral, Bernard; Catherwood, Mark; Airaud, Fabrice; Mansour-Hendili, Lamisse; Hoogewijs, David; Peroni, Edoardo; Idriss, Salam; Lesieur, Valentine; Caillaud, Amandine; Si-Tayeb, Karim; Chariau, Caroline; Gaignerie, Anne; Rab, Minke; Haferlach, Torsten; Meggendorfer, Manja; Bézieau, Stéphane; Benetti, Andrea; Casadevall, Nicole ; Hirsch, Pierre; Rose, Christian; Wemeau, Mathieu; Galacteros, Frédéric; Cassinat, Bruno; Bellosillo, Beatriz; Bento, Celeste ; van Wijk, Richard ; Petrides, Petro E; Randi, Maria Luigia; McMullin, Mary Frances ; Koivunen, Peppi; Girodon, François ; Gardie, Betty articleopenAccess