Severe Hb H Disease Caused by Hb Zürich–Albisrieden (<i>HBA1</i>: c.178G>C): Another Case Report-Reference-Cited by-同舟云学术

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Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report

Published:2022-11-02 Issue:6 Volume:46 Page:341-343
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Wu Shao-Min¹,Huang Su-Ran¹,Li Chan¹,Chen Gui-Lan²,Li Dong-Zhi²

Affiliation:

1. Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, Guangdong Province, People’s Republic of China

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

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2023.2165444

Reference11 articles.

1. The α-Thalassemias

2. Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China

3. Hemoglobin H disease: not necessarily a benign disorder

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

5. Human alpha-globin gene expression. The dominant role of the alpha 2-locus in mRNA and protein synthesis.

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