Pediatric myelofibrosis due to compound heterozygous <i>MPIG6B</i> mutations in a patient of European ancestry-Reference-Cited by-同舟云学术

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Pediatric myelofibrosis due to compound heterozygous MPIG6B mutations in a patient of European ancestry

Published:2022-10-02 Issue:3 Volume:70 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatric Blood & Cancer

Author:

Yenwongfai Leonard N.¹^ORCID,Arora Ranjana¹,Smith Alexander P.¹,Kalfa Theodosia²^ORCID,Husami Ammar²,Radulescu Vlad³,Myers Kasiani²^ORCID,Lorsbach Robert²

Affiliation:

1. Department of Pathology and Laboratory Medicine University of Kentucky College of Medicine Lexington Kentucky USA

2. Cincinnati Children's Cincinnati Ohio USA

3. Pediatric Hematology and Oncology University of Kentucky College of Medicine Lexington Kentucky USA

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.30023

Reference15 articles.

1. Myeloproliferative neoplasms in children

2. CALR mutation screening in pediatric primary myelofibrosis

3. Clinical, histopathologic, and genetic features of pediatric primary myelofibrosis-An entity different from adults

4. Pediatric myelofibrosis: WHO 2024 update on myeloproliferative neoplasms calling?

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