Unlocking thalidomide response as a hemoglobin F augmentation agent in transfusion-dependent β-thalassemia: the genetic impact of BCL11A, HBS1L-MYB, and XmnI polymorphism

Iram Nazir, Muhammad Younus Jamal Siddiqi, Maeesa Wadood, Muhammad Rizwan

Open source

DOI
10.1186/s13000-026-01797-5
Published
2026-07-07
Container
Diagnostic Pathology
Publisher
Springer Science and Business Media LLC
Open access
unknown

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BibTeX

@article{allodium:10.1186/s13000-026-01797-5,
  title = {Unlocking thalidomide response as a hemoglobin F augmentation agent in transfusion-dependent β-thalassemia: the genetic impact of BCL11A, HBS1L-MYB, and XmnI polymorphism},
  author = {Iram Nazir and Muhammad Younus Jamal Siddiqi and Maeesa Wadood and Muhammad Rizwan},
  year = {2026},
  journal = {Diagnostic Pathology},
  doi = {10.1186/s13000-026-01797-5},
  url = {https://doi.org/10.1186/s13000-026-01797-5}
}

RIS

TY  - JOUR
TI  - Unlocking thalidomide response as a hemoglobin F augmentation agent in transfusion-dependent β-thalassemia: the genetic impact of BCL11A, HBS1L-MYB, and XmnI polymorphism
AU  - Iram Nazir
AU  - Muhammad Younus Jamal Siddiqi
AU  - Maeesa Wadood
AU  - Muhammad Rizwan
PY  - 2026
JO  - Diagnostic Pathology
DO  - 10.1186/s13000-026-01797-5
UR  - https://doi.org/10.1186/s13000-026-01797-5
ER  - 

APA

Nazir, I., Siddiqi, M. Y. J., Wadood, M., & Rizwan, M. (2026). Unlocking thalidomide response as a hemoglobin F augmentation agent in transfusion-dependent β-thalassemia: the genetic impact of BCL11A, HBS1L-MYB, and XmnI polymorphism. Diagnostic Pathology. https://doi.org/10.1186/s13000-026-01797-5

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