A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation-Reference-Cited by-同舟云学术

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A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation

Published:2019-03-04 Issue:2 Volume:43 Page:140-144
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Yang Kun¹²^ORCID,Ren Quan²³,Wu Yi²³,Zhou Yali²,Yin Xiaolin²^ORCID

Affiliation:

1. Graduate School of Guangxi University of Chinese Medicine, Nanning, Guangxi Zhuang Autonomous Region, People’s Republic of China;

2. Department of Hematology, The 923rd Hospital of the Peoples Liberation Army, Nanning, Guangxi Zhuang Autonomous Region, People’s Republic of China;

3. Graduate School of Guilin Medical University, Guilin, Guangxi Zhuang Autonomous Region, People’s Republic of China

Funder

the Natural Science Foundation of Guangxi, China

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1620764

Reference20 articles.

1. Hereditary spherocytosis

2. Molecular Genetic Mechanisms of Hereditary Spherocytosis: Current Perspectives

3. New insights on hereditary erythrocyte membrane defects

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

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