References
Kollia P, Kalamaras A, Chassanidis C, Samara M, Vamvakopoulos NK, Radmilovic M, Pavlovic S, Papadakis MN, Patrinos GP (2008) Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the Agamma -158 C>T mutation in gamma-globin gene transcription. Blood Cells Mol Dis 41:263–264
Pavlovic S, Kuzmanovic M, Urosevic J, Poznanic J, Zoranovic T, Djordjevic V, Rasovic N, Bunjevacki G, Cvorkov-Drazic M, Colovic M (2004) Severe central nervous system thrombotic events in hemoglobin Sabine patient. Eur J Haematol 72:67–70
Hull D, Winter PC, McHale CM et al (1998) Familial hemolytic anemia due to Hb Sabine [beta 91(F7)Leu-->Pro] identified by polymerase chain reaction. Hemoglobin 22:263–266
Gasperini D, Galanello R, Melis MA, Iannelli S, Giordano P, Bernini LF, Cao A (1992) Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies. Haematologica 77:381–383
Bogoevski P, Efremov GD, Kezic J, Lam H, Wilson JB, Huisman TH (1983) Hb Sabine or alpha 2 beta 2 91 (F7) Leu----Pro in a Yugoslavian boy. Hemoglobin 7:195–200
Schneider RG, Ueda S, Alperin JB, Brimhall B, Jones RT (1969) Hemoglobin sabine beta 91 (f 7) leu to pro. An unstable variant causing severe anemia with inclusion bodies. N Engl J Med 280:739–745
Susana P, Irma B, Mariana R et al (2015) Severe hemolytic anemia due to de novo Hemoglobin Sabine in an Argentinian newborn. first case in South America. Int Blood Res Rev 3:166–170
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Chen, X., Hu, J., Zhu, J. et al. Severe hemolytic anemia due to combined α thalassemia and de novo Hemoglobin Sabine. Ann Hematol 98, 783–785 (2019). https://doi.org/10.1007/s00277-019-03617-x
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DOI: https://doi.org/10.1007/s00277-019-03617-x