β -thalassemia: New therapeutic modalities, genetics, complications, and quality of life

Mehran Karimi, Sezaneh Haghpanah, Ali T. Taher, Maria Domenica Cappellini

Research output: Contribution to journal › Article

Original languageEnglish
Article number902067
JournalAnemia
Volume2012
DOIs
Publication statusPublished - 2012

ASJC Scopus subject areas

  • Hematology
  • Cell Biology

Cite this

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
Karimi, Mehran ; Haghpanah, Sezaneh ; Taher, Ali T. ; Cappellini, Maria Domenica. / β -thalassemia : New therapeutic modalities, genetics, complications, and quality of life. In: Anemia. 2012 ; Vol. 2012.
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