A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family
Author:
Affiliation:
1. Department of Prenatal Diagnostic Center, Jiangxi Maternal and Child health Hospital, Nanchang, Jiangxi 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/10.1080/03630269.2020.1714648
Reference9 articles.
1. The Molecular Basis of -Thalassemia
2. Beta-thalassemia: from genotype to phenotype
3. Proficiency testing program for hemoglobin E, A2 and F analysis in Thailand using lyophilized hemoglobin control materials
4. The Current Status of β-Thalassemia Major in Mainland China
5. Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China
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1. Wooden-Tip Electrospray Mass Spectrometry Characterization of Human Hemoglobin in Whole Blood Sample for Thalassemia Screening: A Pilot Study;Molecules;2022-06-20
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