A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family-Reference-Cited by-同舟云学术

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A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family

Published:2008-05-01 Issue:5 Volume:93 Page:706-714
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Liu K.,Kralovics R.,Rudzki Z.,Grabowska B.,Buser A. S.,Olcaydu D.,Gisslinger H.,Tiedt R.,Frank P.,Okon K.,van der Maas A. P.C.,Skoda R. C.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 42 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hereditary thrombocythemia due to splicing donor site mutation of THPO in a Japanese family;Annals of Hematology;2023-11-14

2. Genetic background of thrombocytosis in mice mimicking hereditary thrombocytosis in humans;Platelets;2023-11-09

3. Identification of putative noncanonical driver mutations in patients with essential thrombocythemia;European Journal of Haematology;2023-03-14

4. Familial Essential Thrombocythemia With Novel MPL L502G and G208K Mutations;Cureus;2022-03-16

5. Hereditary thrombocytosis: the genetic landscape;British Journal of Haematology;2021-08-02

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