| Literature DB >> 14693843 |
K F S Leung, E S K Ma, A Y Y Chan, L C Chan.
Abstract
Seven patients of Chinese origin who had haemoglobin (Hb) Q-H disease were studied. They were found to have a similar clinical phenotype to that of patients with deletional Hb H disease, who have a near identical genotypic configuration. The complete absence of Hb A in Hb Q-H disease and the similar clinical phenotype to deletional Hb H disease lends support to the observation that Hb Q-Thailand shares similar functional properties with Hb A.Entities:
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Year: 2004 PMID: 14693843 PMCID: PMC1770185 DOI: 10.1136/jcp.57.1.81
Source DB: PubMed Journal: J Clin Pathol ISSN: 0021-9746 Impact factor: 3.411