Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia-Reference-Cited by-同舟云学术

Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia

Published:2018-07-04 Issue:4 Volume:42 Page:236-242
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Dash Preetinanda M.¹²^ORCID,Sahu Praveen K.³^ORCID,Patel Siris²,Mashon Ranjeet S.²⁴^ORCID,Kharat Kiran R.¹^ORCID,Mukherjee Malay B.⁵

Affiliation:

1. Department of Biotechnology, Centre for Advanced Life Sciences, Deogiri College, Aurangabad, Maharashtra, India;

2. Sickle Cell Clinic and Malaria Research Centre, Veer Surendra Sai (VSS) Institute of Medical Sciences and Research, Burla, Sambalpur, Odisha, India;

3. Molecular and Immunology Laboratory, Ispat General Hospital, Rourkela, Odisha, India;

4. Department of Haematopathology, Christian Medical College, Ludhiana, India;

5. Department of Haematogenetics, National Institute of Immuno-Haematology, Parel, Mumbai, India

Funder

Department of Biotechnology , Ministry of Science and Technology

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2018.1536666

Reference36 articles.

1. Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India

2. The Thalassaemia Syndromes

3. Clinical and Molecular Characterization of βSandGγ(Aγδβ)0-Thalassemia in Eastern India

4. Diverse phenotypic expression of sickle cell hemoglobin C disease in an Indian family

5. Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab

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