Hb Sarrebourg beta131(H9)Gln->Arg
CONTACT Internal; alpha1beta1 contact
HEMATOLOGY Iron-deficiency anemia in the carrier
ELECTROPHORESIS Hb X and Hb A separate at alkaline pH; Hb X moves like Hb F, and between Hb F and Hb S on IEF
STRUCTURE STUDIES Not reported in detail; only final data are presented
DNA ANALYSES Not reported; presumed mutation CAG->CGG at codon 131
OCCURRENCE Found in a 9-year-old Turkish boy
OTHER INFORMATION Hb X comprised ~30% of the total Hb
1. Duwig, I., North, M.L., Barth, J.G., Rieffel, M., Nierengarten, P., Arous, N., Riou, J., and Galacteros, F.: Abstract, Nouv. Rev. Fr. d'Hematol., 29:344, 1987.

This material is from the book A Syllabus of Human Hemoglobin Variants (1996) by Titus H.J. Huisman, Marianne F.H. Carver, and Georgi D. Efremov, published by The Sickle Cell Anemia Foundation in Augusta, GA, USA. Copyright © 1996 by Titus H.J. Huisman. All rights reserved. Neither this work nor any part may be reproduced or transmitted in any form or by any means, electronic or mechanical, microfilming and recording, or by any information storage and retrieval systems, without written permission.