Pathogenic “germline” variants associated with myeloproliferative disorders in apparently normal individuals: Inherited or acquired genetic alterations?-Reference-Cited by-同舟云学术

Pathogenic “germline” variants associated with myeloproliferative disorders in apparently normal individuals: Inherited or acquired genetic alterations?

Published:2022-01-03 Issue:3 Volume:101 Page:371-374
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Veitia Reiner A.¹²³⁴,Innan Hideki⁵

Affiliation:

1. Université de Paris Paris France

2. Institut Jacques Monod, CNRS UMR7592 Paris France

3. Université Paris Saclay, CEA Fontenay aux Roses France

4. Institut de Biologie François Jacob, CEA Fontenay aux Roses France

5. Graduate University for Advanced Studies Hayama Japan

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14104

Reference17 articles.

1. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia

2. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

3. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

4. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

5. A Gain-of-Function Mutation ofJAK2in Myeloproliferative Disorders

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