REFERENCES
- Brennan SO, Mathews JRD. Hb Auckland [α87(F8)His→Asn]: a new mutation of the proximal histidine identified by electrospray mass spectrometry. Hemoglobin. 1997;21(5):393–403.
- Brennan SO, Davis RL, Lowen R, Ruskova A. Deletion of five residues from the coiled coil of fibrinogen (Bβ Asn167_Glu171del) associated with bleeding and hypodysfibrinogenemia. Haematologica. 2009;94(4):585–588.
- Brennan SO, Owen MC, Chan T, Ruskova A. Novel hemoglobin α chain elongation resulting from a 15-residue insertion and tandem duplication of the F helix. Clin Biochem. 2008;41(14–15):1156–1161.
- Brennan SO, Ryken S, Chan T. Hb Koya Dora [α142, Term→Ser (TAA>TCA in α2)]: a rare mutation of the α2 gene stop codon associated with α-thalassemia. Hemoglobin. 2010;34(4):402–405.
- Waggoner SA, Liebhaber SA. Regulation of α-globin mRNA stability. Exp Biol Med. 228(4):387–395.
- Yu X, Mollan TL, Butler A, Gow AJ, Olson JS, Weiss MJ. Analysis of human α globin gene mutations that impair binding to the α hemoglobin stabilizing protein. Blood. 2009;113(23):5961–5969.
- Lacerra G, Scarano C, Musollino G, Flagiello A, Pucci P, Carestia C. Hb Foggia or α117(GH5)Phe→Ser: a new α2 globin allele affecting the αHb-AHSP interaction. Haematologica. 2008;93(1):141–142.
- Hajer S, Faid Q, Taieb M, Rachida S, Slaheddine F. First description in Tunisia of a point mutation at codon 119 (CCT→TCT) in the a1 globinL gene: Hb Groene Hart in association with the α3.7 deletion Hemoglobin. 2005;29(4):263–268.