Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients

Heterozygous germline GATA2 mutations strongly predispose to leukemia, immunodeficiency, and/or lymphoedema. We describe a series of 79 patients (53 families) diagnosed since 2011, made up of all patients in France and Belgium, with a follow up of 2249 patients/years. Median age at first clinical sy...

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Gepubliceerd in:Haematologica
Hoofdauteurs: Donadieu, Jean, Lamant, Marie, Fieschi, Claire, de Fontbrune, Flore Sicre, Caye, Aurélie, Ouachee, Marie, Beaupain, Blandine, Bustamante, Jacinta, Poirel, Hélène A., Isidor, Bertrand, Van Den Neste, Eric, Neel, Antoine, Nimubona, Stanislas, Toutain, Fabienne, Barlogis, Vincent, Schleinitz, Nicolas, Leblanc, Thierry, Rohrlich, Pierre, Suarez, Felipe, Ranta, Dana, Chahla, Wadih Abou, Bruno, Bénédicte, Terriou, Louis, Francois, Sylvie, Lioure, Bruno, Ahle, Guido, Bachelerie, Françoise, Preudhomme, Claude, Delabesse, Eric, Cave, Hélène, Bellanné-Chantelot, Christine, Pasquet, Marlène
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Ferrata Storti Foundation 2018
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6068047/
https://ncbi.nlm.nih.gov/pubmed/29724903
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2017.181909
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