Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait-Reference-Cited by-同舟云学术

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Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia Trait

Published:2017-11-02 Issue:4-6 Volume:41 Page:291-292
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Chen Gui-Lan¹,Huang Lv-Yin¹,Zhou Jian-Ying¹,Li Dong-Zhi¹

Affiliation:

1. Guangzhou Women and Children Medical Center affiliated to 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/10.1080/03630269.2017.1398170

Reference6 articles.

1. Mutational spectrum of delta-globin gene in the Portuguese population

2. Known and New δ-Globin Gene Mutations and Other Factors Influencing Hb A2Measurement in the Omani Population

3. Genotype-Phenotype Relationship of the δ-Thalassemia and Hb A2Variants: Observation of 52 Genotypes

4. A novel δ-globin gene mutation (HBD: c.323G>A) masking the diagnosis of β-thalassemia: a first report from India

5. Hb lulu island (α2β2107[G9]Gly→Asp)-β°-thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia

Cited by 3 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. Genetic research and clinical analysis of deletional Chinese Gγ+(Aγδβ)0 -thalassemia and Southeast Asian HPFH in South China;Annals of Hematology;2020-09-15

2. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28

3. Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China;Molecular Genetics & Genomic Medicine;2019-05

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