Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation-Reference-Cited by-同舟云学术

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Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation

Published:2021-03-29 Issue: Volume: Page:1-4
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Wang Rong-Yue¹,Jiang Fan²,Xu Li-Li²,Li Dong-Zhi²

Affiliation:

1. Department of Obstetrics and Gynecology, The Second Affiliated Hospital and Yuying Children’s Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, People’s Republic of China

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

Funder

Guangzhou Institute of Pediatrics/Guangzhou Women and Children’s Medical Center

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2021.1904975

Reference8 articles.

1. Two New α Chain Variants: Hb Die [α93(FG5)Val→Ala (α1)] and Hb Beziers [α99(G6)Lys→Asn (α1)]

2. Hb Bronte or α93(FG5)Val→Gly: A New Unstable Variant of the α2‐Globin Gene, Associated with a Mild α+‐Thalassemia Phenotype

3. Unstable Hemoglobins

4. HB Nottingum or α2β298(F65)VAL→GLY Observed as a De Novo Mutation in a Canadian Child

5. A new unstable hemoglobin mutated in β 98 (FG 5) Val → Ala: Hb Djelfa

Cited by 1 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. Atypical Interference in Hb A1c Measurements Might Be Due to Mosaic Expression of Hemoglobin Variants;Clinical Chemistry;2024-07-03

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