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Severe Clinical Course in a Patient with Congenital Amegakaryocytic Thrombocytopenia Due to a Missense Mutation of the c-MPL Gene

Congenital amegakaryocytic thrombocytopenia (CAMT) generally begins at birth with severe thrombocytopenia and progresses to pancytopenia. It is caused by mutations in the thrombopoietin receptor gene, the myeloproliferative leukemia virus oncogene (c-MPL). The association between CAMT and c-MPL muta...

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Dades bibliogràfiques
Publicat a:Turk J Haematol
Autors principals: Ok Bozkaya, İkbal, Yaralı, Neşe, Işık, Pamir, Ünsal Saç, Rukiye, Tavil, Betül, Tunç, Bahattin
Format: Artigo
Idioma:Inglês
Publicat: Galenos Publishing 2015
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4451487/
https://ncbi.nlm.nih.gov/pubmed/26316487
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/tjh.2013.0191
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