β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey-Reference-Cited by-同舟云学术

β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey

Published:2020-07-03 Issue:4 Volume:44 Page:249-253
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Guzelgul Figen¹,Seydel G. Seyda²^ORCID,Aksoy Kiymet³

Affiliation:

1. Department of Biochemistry, Faculty of Pharmacy, Tokat Gaziosmanpasa University, Tokat, Turkey

2. Zübeyde Hanım Vocational School of Health Services, Nigde Omer Halisdemir University, Nigde, Turkey

3. Department of Medical Biochemistry, Faculty of Medicine, Çukurova University, Adana, Turkey

Funder

State Planning Organization

Çukurova University Research Fund

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2020.1792489

Reference32 articles.

1. Genetic diseases of hemoglobin: diagnostic methods for elucidating β -thalassemia mutations

2. Modell B. World Health Organization. Hereditary diseases programme. 1994. Guidelines for the control of haemoglobin disorders. Geneva, Switzerland: World Health Organization. Available from: https://apps.who.int/iris/handle/10665/66665.

3. Thalassaemia screening in a non-prevalent region of a prevalent country (Turkey): is it necessary?

4. Thalassemias and Hemoglobinopathies in Turkey

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