| Original language | English |
|---|---|
| Article number | 902067 |
| Journal | Anemia |
| Volume | 2012 |
| DOIs | |
| Publication status | Published - 2012 |
ASJC Scopus subject areas
- Hematology
- Cell Biology
Cite this
Karimi, M., Haghpanah, S., Taher, A. T., & Cappellini, M. D. (2012). β -thalassemia: New therapeutic modalities, genetics, complications, and quality of life. Anemia, 2012, [902067]. https://doi.org/10.1155/2012/902067
β -thalassemia : New therapeutic modalities, genetics, complications, and quality of life. / Karimi, Mehran; Haghpanah, Sezaneh; Taher, Ali T.; Cappellini, Maria Domenica.
In: Anemia, Vol. 2012, 902067, 2012.Research output: Contribution to journal › Article
Karimi, M, Haghpanah, S, Taher, AT & Cappellini, MD 2012, 'β -thalassemia: New therapeutic modalities, genetics, complications, and quality of life', Anemia, vol. 2012, 902067. https://doi.org/10.1155/2012/902067
Karimi M, Haghpanah S, Taher AT, Cappellini MD. β -thalassemia: New therapeutic modalities, genetics, complications, and quality of life. Anemia. 2012;2012. 902067. https://doi.org/10.1155/2012/902067
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