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Elyes Slim Ghedira, Serge Pissard. Low fetal hemoglobin rates in patients carrying Thai (δβ)0-deletion and Turkish (δβ)0-deletion/inversion strengthen the hypothesis that the 5′δ BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to “The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia”. haematol [Internet]. 2013Sep.4 [cited 2024Mar.29];98(9):e119-e120. Available from: https://haematologica.org/article/view/6792