Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease-Reference-Cited by-同舟云学术

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Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease

Published:2017-11-02 Issue:4-6 Volume:41 Page:293-296
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Jiang Hua¹,Huang Lv-Yin²,Zhen Li²,Jiang Fan²,Li Dong-Zhi²

Affiliation:

1. Department of Hematology/Oncology, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of China;

2. Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People’s Republic of China

Funder

NSFC

Guangdong Provincial Department of Science and Technology Agency

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2017.1390478

Reference16 articles.

1. Genetic and Clinical Features of Hemoglobin H Disease in Chinese Patients

2. The Hb H Disease Genotypes in Southern China

3. A New Highly Unstable α Chain Variant Causing α+‐Thalassemia: Hb Zurich Albisrieden [α59(E8)Gly→Arg (α2)]

4. Diversity of ?-globin mutations and clinical presentation of ?-thalassemia in Israel

5. Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion

Cited by 5 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. Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report;Hemoglobin;2022-11-02

2. Five novel globin gene mutations identified in five Chinese families by next‐generation sequencing;Molecular Genetics & Genomic Medicine;2021-10-28

3. Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C);Journal of International Medical Research;2021-07

4. Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study;Taiwanese Journal of Obstetrics and Gynecology;2021-07

5. HbH disease due to compound heterozygosity for hemoglobins Zürich‐Albisrieden and Sallanches;Pediatric Blood & Cancer;2020-01-13

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