Clonal evolution in hereditary thrombocytosis with MPL T487A mutation-Reference-Cited by-同舟云学术

Clonal evolution in hereditary thrombocytosis with MPL T487A mutation

Published:2022-08-04 Issue:2 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Vasseur Loic¹^ORCID,Favier Remi²,Kim Rathana³^ORCID,Rabian Florence¹,Cabannes‐Hamy Aurelie⁴,Cassinat Bruno⁵,Maslah Nabih⁵,Vasquez Nadia³,Clappier Emmanuelle³⁶,Kiladjian Jean‐Jacques⁷,Boissel Nicolas¹⁸

Affiliation:

1. Adolescent and Young Adult Hematology Unit Saint‐Louis Hospital Assistance Publique‐Hôpitaux de Paris (AP‐HP) Paris France

2. French National Reference Center for Inherited Platelet Disorders Armand Trousseau Hospital AP‐HP Paris France

3. Hematology Laboratory Saint‐Louis Hospital AP‐HP Paris France

4. Hematology–Oncology Unit Versailles Hospital Le Chesnay France

5. Cellular Biology Laboratory Saint‐Louis Hospital AP‐HP Paris France

6. Université de Paris Saint‐Louis Research Institute INSERM U944/Centre National de la Recherche Scientifique (CNRS) Unité Mixte de Recherche (UMR) 7212 Paris France

7. Clinical Investigation Center Saint‐Louis Hospital AP‐HP Paris France

8. URP‐3518 Saint‐Louis Research Institute Université de Paris Paris France

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.29905

Reference9 articles.

1. Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosis

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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