Novel mechanism of hereditary pyropoikilocytosis phenotype due to co‐inheritance of β globin and α spectrin mutations-Reference-Cited by-同舟云学术

Novel mechanism of hereditary pyropoikilocytosis phenotype due to co‐inheritance of β globin and α spectrin mutations

Published:2021-02-25 Issue:5 Volume:96 Page:
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am J Hematol

Author:

Kim Soo Jin¹^ORCID,Song Jihyun¹,Reading N. Scott²^ORCID,Lautersztain Julio³,Kutlar Abdullah⁴^ORCID,Agarwal Archana M.²,Coetzer Theresa L.⁵,Prchal Josef T.¹

Affiliation:

1. Hematology University of Utah & Huntsman Cancer Center Salt Lake City Utah

2. Department of Pathology ARUP Laboratories Salt Lake City Utah

3. Florida Cancer Specialists and Research Institute Tampa Florida

4. Medical College of Georgia Augusta Georgia

5. Department of Molecular Medicine and Haematology, School of Pathology University of the Witwatersrand Johannesburg South Africa

Funder

National Institutes of Health

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.26121

Reference11 articles.

1. The Molecular Basis of -Thalassemia

2. Codon 104(-G), a dominant 0-thalassemia-like phenotype in a German Caucasian family is associated with mild chronic hemolytic anemia but influenced in severity by co-inherited genetic factors

3. A Congenital Haemolytic Anaemia with Thermal Sensitivity of the Erythrocyte Membrane

4. Erythroblastic Inclusions in Dominantly Inherited β Thalassemias

Cited by 1 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. Molecular insights into hereditary elliptocytosis and pyropoikilocytosis: NGS uncovers multiple potential candidate genes;Annals of Hematology;2023-07-04