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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/16251
Title: Genetic analysis of candidate modifier polymorphisms in Hb E-β<sup>0</sup>-thalassemia patients
Authors: Orapan Sripichai
Johanna Whitacre
Thongperm Munkongdee
Chutima Kumkhaek
Wattanan Makarasara
Pranee Winichagoon
Ken Abel
Andreas Braun
Suthat Fucharoen
The Institute of Science and Technology for Research and Development, Mahidol University
Mahidol University
Sequenom Inc.
Keywords: Arts and Humanities;Biochemistry, Genetics and Molecular Biology;Neuroscience
Issue Date: 1-Jan-2005
Citation: Annals of the New York Academy of Sciences. Vol.1054, (2005), 433-438
Abstract: Hemoglobin E (Hb E)-β-thalassemia patients display a range of clinical severities, from nearly asymptomatic to transfusion-dependent: thalassemia major. Given this clinical heterogeneity, additional genetic factors modifying disease severity remain to be discovered. Association studies are being conducted to elucidate the role of genetic polymorphisms as disease severity modifiers in Hb E-β-thalassemia patients. Using strict scoring criteria, 1060 Hb E-β-thalassemia patients were categorized into mild, moderate, and severe groups. Taking a candidate gene approach, we found no statistically significant differences between the mild and severe patients groups in allelic or genotypic frequencies for single nucleotide polymorphisms within five genes known to influence globin gene expression and erythropolesis. © 2005 New York Academy of Sciences.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=29744446058&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/16251
ISSN: 00778923
Appears in Collections:Scopus 2001-2005

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