Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India-Reference-Cited by-同舟云学术

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Compound heterozygote of Hb DIran [HBB: c.67G>C, β 22(B4) Glu>Gln] with β0-thalassemia [cds 41/42 (-CTTT)] from Eastern India

Published:2018-01 Issue:1 Volume:40 Page:82-85
ISSN:2531-1379
Container-title:Hematology, Transfusion and Cell Therapy
language:en
Short-container-title:Hematology, Transfusion and Cell Therapy

Author:

Mohanty Pradeep Kumar,Meher Satyabrata,Dehury Snehadhini,Bhattacharya Subhra,Das Kishalaya,Patel Siris,Sarkar Biswanath

Funder

National Health Mission of India

Publisher

Elsevier BV

Subject

Hematology,Immunology and Allergy

Reference11 articles.

1. Hemoglobin D Iran: β222 glutamic acid→glutamine (B4);Rahbar;Br J Haematol,1973

2. Regional distribution of beta-thalassemia mutations in India;Verma;Hum Genet,1997

3. Hb Tianshui (HBB: C.119A > G) in compound heterozygosity with Hb S (HBB: C.20A>T) from Odisha, India;Meher;Hemoglobin,2016

4. Hb D-Iran [B22(B4)Glu->Gln] In Southern Italy;De Marco;Hemoglobin,1994

5. An infant with homozygous hemoglobin D-Iran;Thornburg;J Pediatr Hematol Oncol,2001

Cited by 1 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. Unexpected Discovery of Hemoglobin D Iran Families in Punjab, Pakistan by using two different Screening Methods;Pakistan Journal of Medical and Health Sciences;2021-11-30

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