References
- Szelényi JG, Horányi M, Földi J, et al. A new hemoblogin variant in hungary: Hb Savaria − α49 (CE7) Ser->Arg. Hemoglobin. 1980;4(1):27–38.
- Juričić D, Efremov GD, Wilson JB, Huisman THJ. Hb Savaria or α249(CE7)Ser->Argβ2 in a Yugoslavian family. Hemoglobin. 1985;9(6):631–633.
- Ojwang PJ, Ogada T, Webber BB, et al. Hb Savaria or α249(CE7)Ser→Argβ2 in an indigenous female from Kenya. Hemoglobin. 1985;9(2):197–200.
- Suarez CR, Jue DL, Moo-Penn WF. Hemoglobin Savaria − α49(CE7)Ser->Arg in the United States. Hemoglobin. 1985;9(6):627–629.
- Akbari MT, Hamid M. Identification of α-globin chain variants: A report from Iran. Arch Iran Med. 2012;15(9):564–567.
- Srinivasulu S, Acharya AS, Prabhakaran M, et al. HbS-Savaria: The anti-polymerization effect of a single mutation in human alpha-chains. Protein J. 2007;26(8):523–532.
- Patrinos GP, Wajcman H. Commentary − Recording human globin gene variations. Hemoglobin. 2004;28(2):v–vii.
- Riou J, Pissard S, Goossens M, Wajcman H. Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains. Int J Lab Hematol. 2015;37(2):279–286.
- Moradkhani K, Riou J, Wajcman H. Pitfalls in the genetic diagnosis of Hb S. Clin Biochem. 2013;46(4–5):291–299.
- Moradkhani K, Henthorn J, Riou J, et al. Hb Niigata [β1(NA1)Val->Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the Japanese. Hemoglobin. 2007;31(4):477–482.