A NOVEL β0-THALASSEMIA MUTATION AT CODON 55 (−A) AND A RARE 17 bp DELETION AT CODONS 126–131 IN THE INDIAN POPULATION-Reference-Cited by-同舟云学术

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A NOVEL β0-THALASSEMIA MUTATION AT CODON 55 (−A) AND A RARE 17 bp DELETION AT CODONS 126–131 IN THE INDIAN POPULATION

Published:2002-01 Issue:1 Volume:26 Page:41-47
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Nadkarni Anita,Sakaguchi Takehisa,Takaku Hiroshi,Gorakshakar Ajit,Phanasgaonkar Supriya,Colah Roshan B.,Mohanty Dipika,Kiyama Ryoiti

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-120002939

Reference11 articles.

1. Molecular characterization of seven beta-thalassemia mutations in Asian Indians.

2. The spectrum of β-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis

Cited by 13 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. Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia;Annals of Hematology;2020-04-15

2. Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India;Hemoglobin;2019-03-04

3. A Novel 26 bp Deletion [HBB: c.20_45del26bp] in Exon 1 of the β-Globin Gene Causing β-Thalassemia Major;Hemoglobin;2012-01-10

4. A novel β-globin gene deletion (codons 89–93) in a Chinese family;Annals of Hematology;2009-08-05

5. Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population;Blood Cells, Molecules, and Diseases;2009-05

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