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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 1
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Short Communication

Hb F-Avellino [Gγ41(C7)Phe → Leu; HBG2: c.124 T > C]: A New Hemoglobin Variant Observed In A Healthy Newborn

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Pages 61-63 | Received 01 Sep 2015, Accepted 25 Sep 2015, Published online: 16 Nov 2015

References

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  • Kohli-Kumar M, Zwerdling T, Rucknagel DL. Hemoglobin F-Cincinnati, α2Gγ241(C7)Phe → Ser in a newborn with cyanosis. Am J Hematol. 1995;49(1):43–47
  • Prehu C, Behnken LJ, Neumann R, et al. A new unstable hemoglobin variant with low oxygen affinity: Hb Ilmenau [β41(C7)Phe → Cys]. Hemoglobin. 2002;26(2):169–174
  • Burkert LB, Sharma VS, Pisciotta AV, et al. Hemoglobin Mequon β41(C7)Phe → Tyr. Blood. 1976;48(5):645–651
  • Stabler SP, Jones RT, Head C, et al. Hemoglobin Denver [α2β2(41)(C7)Phe → Ser]: A low-O2-affinity variant associated with chronic cyanosis and anemia. Mayo Clin Proc. 1994;69(3):237–243
  • Griffon N, Baudin V, Dieryck W, et al. Tetramer-dimer equilibrium of oxyhemoglobin mutants determined from auto-oxidation rates. Protein Sci. 1998;7(3):673–680
  • Rees DC, Rochette J, Schofield C, et al. A novel silent posttranslational mechanism converts methionine to aspartate in Hemoglobin Bristol (β67[E11]Val-Met → Asp). Blood. 1996;88(1):341–348
  • Kano G, Morimoto A, Hibi S, et al. Hb Bristol-Alesha presenting thalassemia-type hyperunstable hemoglobinopathy. Int J Hematol. 2004;80(5):410–415

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