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Your search keyword '"Iorio E"' showing total 2 results
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2 results on '"Iorio E"'

1. A Swiss family with hemoglobin P Galveston beta117His leads to Arg, including two patients with hb P/beta thalassemia.

Author

Di Iorio EE, Winterhalter KH, Wilson K, Rosenmund A, and Marti HR

Subjects
Amino Acid Sequence, Fetal Hemoglobin analysis, Hemoglobinopathies complications, Hemoglobinopathies genetics, Heterozygote, Humans, Mutation, Pedigree, Switzerland, Hemoglobins, Abnormal analysis, Thalassemia complications
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.

Published
1975
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