Detection of Hb H disease caused by a novel mutation and ‐‐ SEA deletion using capillary electrophoresis-Reference-Cited by-同舟云学术

Detection of Hb H disease caused by a novel mutation and ‐‐ SEA deletion using capillary electrophoresis

Published:2019-06-14 Issue:7 Volume:33 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Li Youqiong¹²^ORCID,Liang Liang²,Tian Mao²,Qin Ting²,Wu Xin²

Affiliation:

1. The Center of Reproduction and Genetic People’s Hospital of Guangxi Zhuang Autonomous Region Nanning Guangxi China

2. The Center of Prenatal Diagnosis People’s Hospital of Guangxi Zhuang Autonomous Region Nanning Guangxi China

Funder

Health Department Research Fund of Guangxi

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.22949

Reference8 articles.

1. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China

2. A laboratory strategy for genotyping haemoglobin H disease in the Chinese

3. α-thalassaemia

4. Novel Point Mutation of the α2-Globin Gene (HBA2) and a Rare 2.4 kb Deletion of the α1-Globin Gene (HBA1), Identified in Two Chinese Patients with Hb H Disease

5. Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family

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3. Identification of a Novel Hb H Disease with Glucose-6-Phosphate Dehydrogenase Deficiency Using Whole Genome Sequencing;Hemoglobin;2022-05-04

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