Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim

Congenital amegakaryocytic thrombocytopenia (CAMT) is an inherited disorder characterized at birth by thrombocytopenia with reduced megakaryocytes, which evolves into generalized bone marrow aplasia during childhood. Although CAMT is genetically heterogeneous, mutations of MPL, the gene encoding for...

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Detalles Bibliográficos
Autores principales: Pecci, Alessandro, Ragab, Iman, Bozzi, Valeria, De Rocco, Daniela, Barozzi, Serena, Giangregorio, Tania, Ali, Heba, Melazzini, Federica, Sallam, Mohamed, Alfano, Caterina, Pastore, Annalisa, Balduini, Carlo L, Savoia, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760853/
https://www.ncbi.nlm.nih.gov/pubmed/29191945
http://dx.doi.org/10.15252/emmm.201708168

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760853/
https://www.ncbi.nlm.nih.gov/pubmed/29191945
http://dx.doi.org/10.15252/emmm.201708168

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