Identification of a Novel δ-Globin Gene Mutation in an Iranian Family-Reference-Cited by-同舟云学术

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Identification of a Novel δ-Globin Gene Mutation in an Iranian Family

Published:2010-11-15 Issue:6 Volume:34 Page:594-598
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Amirian Azam,Jafarinejad Masoomeh,Kordafshari Alireza R.,Mosayyebzadeh Marjan,Karimipoor Morteza,Zeinali Sirous

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2010.528323

Reference11 articles.

1. The Thalassaemia Syndromes

2. Delta +-thalassemia in Sardinia

3. Homozygous Delta-Thalassemia First Discovered in Japanese Family With Hereditary Persistence of Fetal Hemoglobin

4. Homozygous Delta Thalassemia in Japan

5. The IVS-II-1 (G → A) β0-Thalassemia Mutation inCISwith Hb A2-Troodos [δ116(G18)Arg → Cys (CGC →TGC)] Causes a Complex Prenatal Diagnosis in an Iranian Family

Cited by 6 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. In silico prediction of HBD gene variants in the Iranian population;Egyptian Journal of Medical Human Genetics;2021-03-01

2. Molecular epidemiology, pathogenicity, and structural analysis of haemoglobin variants in the Yunnan province population of Southwestern China;Scientific Reports;2019-06-04

3. Analysis of deletional hereditary persistence of fetal hemoglobin/δβ‐thalassemia and δ‐globin gene mutations in Southerwestern China;Molecular Genetics & Genomic Medicine;2019-05

4. Results of Coexistence of β-Thalassemia Minor in Hb H Disease Patients;Hemoglobin;2018-11-02

5. Molecular Characterization ofδ-Thalassemia in Iran;Hemoglobin;2016-01-02

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