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Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis

Title: Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis
Authors: CDL Rode cel; Circulatory Health; CDL Cluster Speciële Diagnostiek; Child Health; Delamare, 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; ECYT-3 consortium
Publisher Information: Ferrata Storti Foundation 2023-11-01
Document Type: Electronic Resource
Index Terms: Article; Peer reviewed; Publisher version; Published
URL: https://doi.org/10.3324/haematol.2023.282913; http://hdl.handle.net/1874/460179; https://dspace.library.uu.nl/handle/1874/460179; 0390-6078; Haematologica; 108; 11; 3068; 3085
Availability: Open access content. Open access content; Open Access (free)
Note: English
Other Numbers: QGJ oai:dspace.library.uu.nl:1874/460179; Delamare, M, Le Roy, A, Pacault, M, Schmitt, L, Garrec, C, Maaziz, N, Myllykoski, M, Rimbert, A, Karaghiannis, V, Aral, B, Catherwood, M, Airaud, F, Mansour-Hendili, L, Hoogewijs, D, Peroni, E, Idriss, S, Lesieur, V, Caillaud, A, Si-Tayeb, K, Chariau, C, Gaignerie, A, Rab, M, Haferlach, T, Meggendorfer, M, Bézieau, S, Benetti, A, Casadevall, N, Hirsch, P, Rose, C, Wemeau, M, Galacteros, F, Cassinat, B, Bellosillo, B, Bento, C, Van Wijk, R, Petrides, P E, Randi, M L, McMullin, M F, Koivunen, P, Girodon, F, Gardie, B & ECYT-3 consortium 2023, 'Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis', Haematologica, vol. 108, no. 11, pp. 3068-3085. https://doi.org/10.3324/haematol.2023.282913; URN:NBN:NL:UI:10-1874-460179; 536471043; 1521265407
Contributing Source: UNIVERSITEIT UTRECHT; From OAIster®, provided by the OCLC Cooperative.
Accession Number: edsoai.on1521265407
Database: OAIster