Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations-Reference-Cited by-同舟云学术

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Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations

Published:2023-03-04 Issue:2 Volume:47 Page:52-55
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Qiu Yuling¹²³,Wei Shilu²³,Hou Wei²³,Lai Ketong²³,Zhu Hengying²³,Li Wenwei²³,Li Qi²³,Yang Zheng¹,Shu Qisheng¹,Chen Ping²³,Mo Wuning¹^ORCID

Affiliation:

1. Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, China

2. Guangxi Key Laboratory of Thalassemia Research, Guangxi Medical University, Nanning, China

3. NHC Key Laboratory of Thalassemia Medicine, Guangxi Medical University, Nanning, China

Funder

Guangxi Project of Scientific Research Basic Capacity Improvement of Young and Middle-aged College Teachers

Open Project of NHC Key Laboratory of Thalassemia Medicine

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2023.2219008

Reference13 articles.

1. The prevalence and spectrum of and thalassaemia in Guangdong Province: implications for the future health burden and population screening

2. Thalassaemia

3. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China

4. Clinical features and molecular analysis in Thai patients with HbH disease

5. Results of Coexistence of β-Thalassemia Minor in Hb H Disease Patients

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. Reliability of hemoglobin A₂ value as measured by the Premier Resolution system for screening of β-thalassemia carriers;Clinical Chemistry and Laboratory Medicine (CCLM);2023-10-17

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