A combination of the (αα) GZ and ‐‐ SEA deletions causing a severe form of hemoglobin H disease-Reference-Cited by-同舟云学术

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A combination of the (αα) GZ and ‐‐ SEA deletions causing a severe form of hemoglobin H disease

Published:2019-11-22 Issue:2 Volume:42 Page:
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Cheng Yi¹^ORCID,Cai Decheng¹,Shang Xuan¹^ORCID,Pang Dejian¹,Wei Xiaofeng¹,Zhong Jianmei¹,Xu Xiangmin¹²³

Affiliation:

1. Department of Medical Genetics School of Basic Medical Sciences Southern Medical University Guangzhou China

2. Guangdong Genetics Testing Engineering Research Center Guangzhou China

3. Guangdong Provincial Key Laboratory of Single Cell Technology and Application Guangzhou China

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.13122

Reference12 articles.

1. Thalassaemia

2. Molecular Basis and Genetic Modifiers of Thalassemia

3. Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia

4. Manipulating the Mouse Genome to Engineer Precise Functional Syntenic Replacements with Human Sequence

5. A novel selective deletion of the major α-globin regulatory element (MCS-R2) causing α-thalassaemia

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. Molecular characterization of a novel 83.9-kb deletion of the α-globin upstream regulatory elements by long-read sequencing;Blood Cells, Molecules, and Diseases;2023-11

2. Identification of a novel 91.5 kb-deletion (αα) ^FJ in the α-globin gene cluster using single-molecule real-time (SMRT) sequencing;The Journal of Maternal-Fetal & Neonatal Medicine;2023-09-06

3. Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis;Hemoglobin;2020-07-03

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