Hereditary α tryptasemia is a valid genetic biomarker for severe mediator-related symptoms in mastocytosis

Mastocytosis is a hematopoietic neoplasm characterized by expansion of KIT D816V-mutated clonal mast cells in various organs and severe or even life-threatening anaphylactic reactions. Recently, hereditary α-tryptasemia (HαT) has been described as a common genetic trait with increased copy numbers o...

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Publicat a:Blood
Autors principals: Greiner, Georg, Sprinzl, Bettina, Górska, Aleksandra, Ratzinger, Franz, Gurbisz, Michael, Witzeneder, Nadine, Schmetterer, Klaus G., Gisslinger, Bettina, Uyanik, Goekhan, Hadzijusufovic, Emir, Esterbauer, Harald, Gleixner, Karoline V., Krauth, Maria T., Pfeilstöcker, Michael, Keil, Felix, Gisslinger, Heinz, Nedoszytko, Boguslaw, Niedoszytko, Marek, Sperr, Wolfgang R., Valent, Peter, Hoermann, Gregor
Format: Artigo
Idioma:Inglês
Publicat: 2021
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7116780/
https://ncbi.nlm.nih.gov/pubmed/32777817
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood.2020006157
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