Molecular and Hematological Characterization of Two Novel δ-Globin Gene Mutations Found in Chinese Individuals
Author:
Affiliation:
1. Prenatal Diagnosis Center, Dongguan Maternal and Child Health Hospital, Dongguan, Guangdong Province, People’s Republic of China
Funder
Social Developmental Project of Dongguan City
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2018.1458628
Reference10 articles.
1. The role of haemoglobin A2 testing in the diagnosis of thalassaemias and related haemoglobinopathies
2. δ-Thalassemia in Cyprus
3. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China
4. Analysis Of δ-Globin Gene Mutations in the Chinese Population
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1. First report of the spectrum of δ‐globin gene mutations among women of reproductive age in Fujian area—Discrimination of δ‐thalassemia, α‐thalassemia, and Iron Deficiency Anemia;Journal of Clinical Laboratory Analysis;2020-09-09
2. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia;BMC Pediatrics;2019-02-18
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