A Compound Heterozygous Asian Indian Inversion Deletion Gγ(Aγδβ) with β-Thalassemia in Central India: A Case Report.
作者信息
Lad Harsha, Ghanghoria Pawan, Yadav Rajiv, Patel Purushottam, Gwal Anil, Shanmugam Rajasubramaniam
机构信息
1National Institute for Research in Tribal Health (Indian Council of Medical Research), Nagpur Road, Jabalpur, 482003 Madhya Pradesh India.
2Department of Paediatrics, Netaji Subhash Chandra Bose Medical College, Jabalpur, India.
出版信息
Indian J Hematol Blood Transfus. 2018 Jan;34(1):185-187. doi: 10.1007/s12288-017-0806-z. Epub 2017 Mar 27.
Abstract
摘要
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本文引用的文献
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Compound heterozygous state of β-thalassemia with IVS1-5 (G→C) mutation and Indian deletion-inversion Gγ(Aγδβ)(0)-thalassemia in eastern India.
Rev Bras Hematol Hemoter. 2015 May-Jun;37(3):202-6. doi: 10.1016/j.bjhh.2014.12.002. Epub 2015 May 12.
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Haematological characterisation and molecular basis of asian Indian inversion deletions delta Beta thalassemia: a case report.
J Clin Diagn Res. 2014 Sep;8(9):FD01-2. doi: 10.7860/JCDR/2014/8362.4776. Epub 2014 Sep 20.
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Phenotypic heterogeneity of asian Indian inversion deletions gγ(aγδβ)0 breakpoint a and breakpoint B.
Indian J Clin Biochem. 2013 Jan;28(1):98-101. doi: 10.1007/s12291-012-0232-9. Epub 2012 Jun 15.
4
Molecular characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population.
Hemoglobin. 2008;32(5):425-33. doi: 10.1080/03630260802341687.
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Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
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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. 2001 Nov;25(4):397-407. doi: 10.1081/hem-100107877.
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