Clinical and molecular genetic analysis of a Chinese family with hereditary elliptocytosis caused by a novel mutation in the EPB41 gene-Reference-Cited by-同舟云学术

Clinical and molecular genetic analysis of a Chinese family with hereditary elliptocytosis caused by a novel mutation in the EPB41 gene

Published:2021-05-04 Issue: Volume: Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Cao Manxiong¹,Huang Zhanqin²,Zhou Huanbing³,Lin Jinghua³,Zhang Dongqing³^ORCID

Affiliation:

1. Department of Hematology the First Affiliated Hospital of Shantou University Medical College Shantou P.R. China

2. Department of Pharmacology Shantou University Medical College Shantou P.R. China

3. Department of Laboratory Medicine the First Affiliated Hospital of Shantou University Medical College Shantou P.R. China

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry, medical,Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.23781

Reference18 articles.

1. Hereditary elliptocytosis: spectrin and protein 4.1R;Gallagher PG;Semin Hematol,2004

2. Spectrin‐based skeleton in red blood cells and malaria;Dhermy D;Curr Opin Hematol,2007

3. Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin;Glele‐Kakai C;Br J Haematol,1996

4. Characteristics of red cell membrane disorders in the Japanese population;Yawata Y;Rinsho Byori,1997

5. Hereditary hemolytic anemia in Korea from 2007 to 2011: A study by the Korean Hereditary Hemolytic Anemia Working Party of the Korean Society of Hematology;Park ES;Blood Res,2013

Cited by 2 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. Case report: Whole-exome sequencing for a hereditary elliptocytosis case with an unexpectedly low HbA1c;Frontiers in Medicine;2023-12-12

2. A Systematic review on diagnostic methods of red cell membrane disorders in Asia;International Journal of Laboratory Hematology;2022-01-23