Journal article
Hemoglobin QIndia, α64(E l3) Asp→His, and β- Thalassemiaina Canadian Family
Abstract
Cellulose acetate electrophoresis at pH 8.4 showed a hemoglobin variant with the mobility of hemoglobin S in a Canadian family. Sequence analysis revealed that histidine was substituted for aspartic acid at position 64 in the alpha-chain. This variant was found in association with a beta-thalassemia trait condition.
Authors
Schmidt RM; Bechtel KC; Moo-Penn WF
Journal
American Journal of Clinical Pathology, Vol. 66, No. 2, pp. 446–448
Publisher
Oxford University Press (OUP)
Publication Date
August 1, 1976
DOI
10.1093/ajcp/66.2.446
ISSN
0002-9173