First observation of hemoglobin M Saskatoon (ß63 (E7) His>Tyr(C-T)) in the Iraqi population

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1. Huismann THJ, Carver MFH, Efremov GDA. Syllabus of hemoglobin variants. The Sickle Cell Anemia Foundation. 2nd ed. GA, USA: Augusta, 1998 2. Vella F, Kamuzora H, Lehmann H, Duncan B, Harold W. A second family with hemoglobin M Saskatoon in Saskatchewan. Clin Biochem 1974; 7 (2): 186-191 3. Nagai M, Yoneyama Y. Reduction of methemoglobins M Hyde Park, M Saskatoon and M Milwaukee by ferredoxin and ferredoxin-nicotinamide adenine dinucleotide phosphate reductase system. J Biol Chem 1983; 258 (23): 14379-14384 4. Arbane-Dahmane M, Rouabhi F, Hocine M, Benabadji M, Redad M, Blouquit Y, Arous N, Delanoe-Garin J, Riou J, Lacombe C. Hemoglobin M Saskatoon (alpha 2 beta 2 63(E7) His----Tyr) in an Algerian family. Hemoglobin 1985; 9 (5): 509-511 5. Waye JS, Patterson M, Eng B. De novo beta-globin gene mutation [beta 63(E7)His-->Tyr] giving rise to Hb M disease in a Newfoundlander. Hemoglobin 1994; 18 (6): 441-443 6. Suryantoro P, Takeshima Y, Haryanto A, Matsuo M. C to T transition at the first nucleotide of codon 63 of the beta- globin gene corresponding to hemoglobin M-Saskatoon in an Indonesian boy. Jpn J Hum Genet 1995; 40 (2): 195-201 7. Hütten M, Kohne E, Yagmur E, Schaible T, Wenzl T, Wagner N, Heimann K. Persistent cyanosis in a 4 month old infant with severe pneumonia and haemoglobin M. Klin Padiatr 2009; 221 (5): 305-307 8. Kedar PS, Nadkarni AH, Phanasgoankar S, Madkaikar M, Ghosh K, Gorakshakar AC, Colah RB, Mohanty D. Congenital methemoglobinemia caused by Hb-MRatnagiri (β-63CAT→TAT, His→Tyr) in an Indian family. Am J Hematol 2005; 79 (2): 168-170 9. Brunner-Agten S, Hergersberg M, Herklotz R, Hirt A, Huber AR. Compound heterozygosity of Hb Hamilton and de novo mutated HbM Saskatoon. Ann Hematol 2010; 89 (5): 517- 518 10. Altay Ç. Abnormal Hemoglobins in Turkey. Turk J Haematol 2002; 19: 63-74 11. Akar E, Akar N. A review of abnormal hemoglobins in Turkey. Turk J Hematol 2007: 24; 2-3 12. Özsoylu Ş. Congenital methemeoglobinemia due to hemoglobin M. Acta Haematol 1972; 47: 225-232 13. Mast A, Milo R, Junien C, Leroux A, Krishnamoorthy R, Wajcman H, Labie D, Kaplan JC. Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotes. Acta Haematol 1976; 56 (3): 174-182