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Hemoglobin
international journal for hemoglobin research
Volume 10, 1986 - Issue 2
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Original Article

HB M iwate [α287His→Tyrβ2]: De novo mutation in an irish family

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Pages 205-208 | Received 09 Oct 1985, Accepted 02 Jan 1986, Published online: 07 Jul 2009

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Chungwoo Shin, Mee Hong, Myungshin Kim & Jung Hyun Lee. (2019) Exon sequencing of the alpha-2-globin gene for the differential diagnosis of central cyanosis in newborns: a case report. BMC Pediatrics 19:1.
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Ganesh Kumar V, Prashant Sharma, Sanjeev Chhabra, Jasbir Kaur Hira, Amita Trehan & Reena Das. (2015) Hb M-Iwate in an Indian family. Clinica Chimica Acta 446, pages 192-194.
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Marcos Borato Viana & André Rolim Belisário. (2014) De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth. Revista Brasileira de Hematologia e Hemoterapia 36:3, pages 230-234.
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Chunjiang Zhu, Wenfang Yu, Jiansheng Xie, Ling Chen, Hui Ding, Xuan Shang & Xiangmin Xu. (2010) Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boy. Blood Cells, Molecules, and Diseases 45:3, pages 223-226.
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Kiran V. Sarikonda, Rubens S. Ribeiro, Jennifer L. Herrick & James D. Hoyer. (2009) Hemoglobin lansing: A novel hemoglobin variant causing falsely decreased oxygen saturation by pulse oximetry. American Journal of Hematology 84:8, pages 541-541.
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