A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation

Author:

Singha Kritsada,Tepakhan Wanicha,Yamsri Supawadee,Chaibunruang Attawut,Srivorakun Hataichanok,Pansuwan Anupong,Fucharoen Goonnapa,Fucharoen SupanORCID

Funder

Mahasarakham University

Thailand Science Research and Innovation

Thailand Research Fund

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference49 articles.

1. The Thalassemia Syndromes;Weatherall,2001

2. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management;Steinberg,2009

3. Molecular basis and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in Thailand;Panyasai;Haematologica,2004

4. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer;Prakobkaew;Eur. J. Haematol.,2014

5. Molecular basis of non-deletional HPFH in Thailand and identification of two novel mutations at the binding sites of CCAAT and GATA-1 transcription factors;Singha;Sci. Rep.,2023

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