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Modifying effect of XmnI, BCL11A, and HBS1L-MYB on clinical appearances: A study on β-thalassemia and hemoglobin E/β-thalassemia patients in Indonesia.

Hematology/oncology and stem cell therapy - 1 Jun 2016

Rujito Lantip, Basalamah Muhammad, Siswandari Wahyu, Setyono Joko, Wulandari Gondo, Mulatsih Sri, Sofro Abdul Salam M, Sadewa Ahmad Hamim, Sutaryo Sutaryo

Abstract excerpt

OBJECTIVE/BACKGROUND: Thalassemia is a monogenic hematologic disease that has the highest prevalence globally. In addition, there is complexity of the genetic background associated with a variety of phenotypes presented among patients. Genetic heterogeneity related to fetal hemoglobin (HbF) production has been reported as an influencing phenotypic factor of β-thalassemia (β-thal). Therefore, this study aimed to...

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PMID: 27009595
DOI: 10.1016/j.hemonc.2016.02.003

Genes

MYB

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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