Hemoglobinopathies and Thalassemias

Author:

Peslak Scott,Sayani Farzana

Publisher

Elsevier

Reference75 articles.

1. The thalassemia syndromes;Weatherall,2001

2. Unstable hemoglobins, hemoglobins with altered oxygen affinity, hemoglobin M, and other variants of clinical and biological interest;Steinberg,2009

3. An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level;Bauer;Science,2013

4. DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease;Lettre;Proc Natl Acad Sci U S A,2008

5. Direct promoter repression by BCL11A controls the fetal to adult hemoglobin switch;Liu;Cell,2018

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