Profiling of 35 Cases of Hb S/Hb E (<i>HBB</i>: c.20A>T/<i>HBB</i>: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India-Reference-Cited by-同舟云学术

Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India

Published:2021-11-02 Issue:6 Volume:45 Page:380-386
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Dehury Snehadhini¹²^ORCID,Mohanty Pradeep K.¹³^ORCID,Patel Siris¹,Meher Satyabrata¹^ORCID,Das Kishalaya¹,Purohit Prasanta⁴^ORCID,Sahoo Sarmila¹,Ratha Jagnyeswar²

Affiliation:

1. Sickle Cell Institute, Sickle Cell Project (National Health Mission Odisha), Veer Surendra Sai Institute of Medical Science and Research (VIMSAR), Burla, Sambalpur, Odisha, India

2. School of Life Sciences, Sambalpur University, Jyoti Vihar, Burla, Sambalpur, Odisha, India

3. Department of Medicine, VIMSAR, Burla, Sambalpur, Odisha, India

4. Multi-Disciplinary Research Unit, Maharaja Krishna Chandra Gajapati (MKCG) Medical College, Berhampur, Odisha, India

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2021.1965618

Reference44 articles.

1. Sickle cell disease in India

2. Greer JP, Foerster J, Lukens JN, et al., Editors. Abnormal hemoglobins: general considerations. Wintrobe's Clinical Hematology, 11th ed. Philadelphia (PA): Lippincott Williams & Wilkins. 2004:1247–1262.

3. The First Observation of Sickle-Cell Hæmoglobin E Disease

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