| Literature DB >> 1164567 |
E E Di Iorio, K H Winterhalter, K Wilson, A Rosenmund, H R Marti.
Abstract
The mutant Hb P Galveston (beta117His leads to Arg) is observed in two heterozygotes for beta thalassemia and by itself does not cause clinical symptoms. Some of the physico-chemical properties of Hb P Galveston are identical to the onemical properties of Hb P Galveston are identical to the ones hemoglobin Zurich (beta 63 His leads to Arg) so that only a detailed analysis led to its proper identification.Entities:
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Year: 1975 PMID: 1164567 DOI: 10.1007/bf01633721
Source DB: PubMed Journal: Blut ISSN: 0006-5242