Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (<i>HBB</i>: c.393delT)-Reference-Cited by-同舟云学术

Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)

Published:2022-06-10 Issue:4 Volume:46 Page:253-255
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Lin Xiao-Mei¹,Jiang Fan¹,Li Jian¹,Li Dong-Zhi¹

Affiliation:

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

Funder

Guangzhou Institute of Pediatrics/Guangzhou Women and Children’s Medical Center, 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/10.1080/03630269.2022.2072325

Reference14 articles.

1. β-Thalassemia

2. Dominantly Transmitted β-Thalassemia Arising From the Production of Several Aberrant mRNA Species and One Abnormal Peptide

3. IS IT DOMINANTLY INHERITED β THALASSAEMIA OR JUST A β-CHAIN VARIANT THAT IS HIGHLY UNSTABLE?

4. A KOREAN FAMILY WITH A DOMINANTLY INHERITED β-THALASSEMIA DUE TO Hb DURHAM-N.C./BRESCIA [β114(G16)Leu→Pro]

5. Dominantly inherited thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the globin gene: Hb morgantown ( 91 CTG>CG)

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