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- Comment in:
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N Engl J Med. 2008 Jul 3;359(1):98; author reply 98-9.
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N Engl J Med. 2008 Jul 3;359(1):98; author reply 98-9.
Hydroxyurea for the treatment of sickle cell anemia.
Department of Laboratory Medicine, Children's Hospital Boston, MA 02115, USA. orah.platt@childrens.harvard.edu
PMID: 18367739 [PubMed - indexed for MEDLINE]
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Cited by 1 PubMed Central article
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DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.
Lettre G, Sankaran VG, Bezerra MA, Araújo AS, Uda M, Sanna S, Cao A, Schlessinger D, Costa FF, Hirschhorn JN, et al.
Proc Natl Acad Sci U S A. 2008 Aug 19; 105(33):11869-74. Epub 2008 Jul 30.
[Proc Natl Acad Sci U S A. 2008]