Article
Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.
The pharmacogenomics journal - 1 Dec 2007
Ma Q, Wyszynski D F, Farrell J J, Kutlar A, Farrer L A, Baldwin C T, Steinberg M H
Abstract excerpt
The increase in fetal hemoglobin (HbF) in response to hydroxyurea (HU) varies among patients with sickle cell anemia. Twenty-nine candidate genes within loci previously reported to be linked to HbF level (6q22.3-q23.2, 8q11-q12 and Xp22.2-p22.3), involved in metabolism of HU and related to erythroid progenitor proliferation were studied in 137 sickle cell anemia patients treated with HU. Three-hundred and twenty...
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