| Literature DB >> 23105893 |
Vijay S Bhat1, K K Dewan, P R Krishnaswamy, A K Mandal, P Balaram.
Abstract
Hemoglobin Q- India (alpha) 64 Asp → His is an alpha chain variant which is generally found in heterozygous state and presents normal hematological blood picture. Here we report a rare case of HbQ-India with a thalassemic phenotype that has been analyzed using a combination of mass spectrometry, gene sequencing and PCR analysis. This combined analyses revealed the HbQ variant to be associated with a beta chain mutation, IVS 1-1 [G>T]. Though HbQ has earlier been reported with thalassemic trait using different techniques, this is the first report of a compound α and β chain Hb heterozygous mutant involving HbQ and IVS1-1 being validated using Mass Spectrometry and Reverse dot blot hybridization.Entities:
Keywords: Amplification Refractory Mutation System; Hemoglobin Q; Intervening sequence; Mass Spectrometry; Reverse dot blot hybridization
Year: 2010 PMID: 23105893 PMCID: PMC3453018 DOI: 10.1007/s12291-010-0020-3
Source DB: PubMed Journal: Indian J Clin Biochem ISSN: 0970-1915