Neutrophil specific granule and NETosis defects in gray platelet syndrome

Gray platelet syndrome (GPS) is an autosomal recessive bleeding disorder characterized by a lack of α-granules in platelets and progressive myelofibrosis. Rare loss-of-function variants in neurobeachin-like 2 (NBEAL2), a member of the family of beige and Chédiak-Higashi (BEACH) genes, are causal of...

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Detaylı Bibliyografya
Yayımlandı:Blood Adv
Asıl Yazarlar: Aarts, Cathelijn E. M., Downes, Kate, Hoogendijk, Arie J., Sprenkeler, Evelien G. G., Gazendam, Roel P., Favier, Rémi, Favier, Marie, Tool, Anton T. J., van Hamme, John L., Kostadima, Myrto A., Waller, Kate, Zieger, Barbara, van Bergen, Maaike G. J. M., Langemeijer, Saskia M. C., van der Reijden, Bert A., Janssen, Hans, van den Berg, Timo K., van Bruggen, Robin, Meijer, Alexander B., Ouwehand, Willem H., Kuijpers, Taco W.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Hematology 2021
Konular:
Phagocytes, Granulocytes, and Myelopoiesis
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7839360/
https://ncbi.nlm.nih.gov/pubmed/33496751
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2020002442
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