A Compound Heterozygous Asian Indian Inversion Deletion Gγ(Aγδβ)0 with β-Thalassemia in Central India: A Case Report
Author:
Funder
Indian Council of Medical Research
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
http://link.springer.com/article/10.1007/s12288-017-0806-z/fulltext.html
Reference7 articles.
1. Old JM, Khan SN, Verma I, Fucharoen S, Kleanthous M, Ioannou P, Kotea N, Fisher C, Riazuddin S, Saxena R, Winichagoon P, Kyriacou K, Al-Quobaili F, Khan B (2001) A multi-center study in order to further define the molecular basis of beta-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction. Hemoglobin 25:397–407
2. Craig JE, Barneson RA, Prior J, Raven L, Thein SL (1994) Rapid detection of deletions causing δβ thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood 83:1673–1682
3. Supan F, Yutthana P, Satja S, Goonnapa F, Kanokwan S (2002) Molecular and hematological characterization of hereditary persistence of fetal hemoglobin-6/Indian deletion–inversion Gγ(Aγδβ)0-thalassemia and Gγ(Aγδβ)0-thalassemia/HbE in Thai patients. Am J Hematol 71:109–113
4. Kunger JM, Gupta M, Singh R, Kapoor R, Pandey HR (2014) Haematoligical characterization and molecular basis of Asia India inversion deletion delta beta thalassemia: a case report. J Clin Diagn Res. 8(9):FD01–FD02. doi: 10.7860/JCDR/2014/8362.4776
5. Nadkarni A, Wadia M, Gorakshakar A, Kiyama R, Colah RB, Mohanty D (2008) Molecular characterization of δβ thalassemia and hereditary persistence of fetal hemoglobin in the Indian population. Hemoglobin 32:425–433
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