| Literature DB >> 11422231 |
K F Leung1, W Y Au, A Y Chan, L C Chan, J S Waye, D H Chui, S K Ma.
Abstract
A Chinese family with concurrent hereditary spherocytosis (HS) and haemoglobin (Hb) Q-Thailand is described. The Hb Q-Thailand mutation was found on the remaining alpha1 globin gene on a chromosome 16 containing the (-alpha 4.2) deletion. Active haemolysis in members of this family is segregated with the HS phenotype, and the Hb Q-Thailand in the heterozygous state does not seem to show any modulating effect on HS.Entities:
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Year: 2001 PMID： 11422231 DOI： 10.1046/j.1365-2257.2001.00349.x
Source DB: PubMed Journal: Clin Lab Haematol ISSN： 0141-9854