Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India-Reference-Cited by-同舟云学术

Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India

Published:2019-03-04 Issue:2 Volume:43 Page:132-136
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Dehury Snehadhini¹^ORCID,Meher Satyabrata¹^ORCID,Patel Siris¹,Das Kishalaya¹,Jana Arpita²,Bhattacharya Subhra²,Sahoo Sarmila¹,Sarkar Biswanath²,Mohanty Pradeep K.¹³

Affiliation:

1. Odisha Sickle Cell Project (NHM), Sickle Cell Institute, Veer Surendra Sai Institute of Medical Science and Research (VIMSAR), Burla, Sambalpur, Odisha State, India;

2. Anthropological Survey of India, 4th Floor, Spirit Building, Kolkata, West Bengal State, India;

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

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1602052

Reference15 articles.

1. Geographic and Ethnic Distribution of β-Thalassemia Mutations in Uttar Pradesh, India

2. Prevalence of Deletional Alpha Thalassemia and Sickle Gene in a Tribal Dominated Malaria Endemic Area of Eastern India

Cited by 3 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. Evaluation of pharmacological efficacy and safety of hydroxyurea in sickle cell disease: Study of a pediatric cohort from Chhattisgarh, India;Pediatric Hematology and Oncology;2022-10-13

2. 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;Hemoglobin;2021-11-02

3. 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