A second case of Hb Bologna-St. Orsola [β146(HC3)His → Tyr] in an unrelated family of anglo-celtic origin

Hemoglobin

Volumn 24, Issue 2, 2000, Pages 139-142

  Gilbert, Anne T ^a   Fleming, P J ^a   Hertzberg, M S ^a  

^a WESTMEAD HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; HEMOGLOBIN VARIANT;

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; DNA DETERMINATION; HEMOGLOBIN ANALYSIS; HEMOGLOBINOPATHY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; MALE; OXYGEN AFFINITY; SCHOOL CHILD;

EID: 0034045270     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630260009003433     Document Type: Article

References (5)

1. Ivaldi, G., David, O., Paradossi, V., Baffico, M., Scime Degani, V., Leone, D., Baldi, M., Parodi, M.I., Bernardi, P., and Ricco, G.: Hb Bologna-St. Orsola [β146(HC3)His → Tyr]: a new high oxygen affinity variant with halved Bohr effect and highly reduced reactivity towards 2,3-diphosphoglycerate. Hemoglobin, 23:353-360, 1999.
2. Th edition, Churchill Livingstone, London, England, 1991.
3. Sack, J.S., Andrews, L.C., Magnus, K.A., Hanson, J.C., Rubin, J., and Love, W.E.: Location of amino residues in human deoxyhemoglobin. Hemoglobin, 2:153-69, 1978.
4. Dickerson, R.E. and Geis, I.: Hemoglobin: Structure, Function, Evolution and Pathology, The Benjamin/Cummings Publishing Company, Inc., Merlo Park, USA, 1983.
5. Shih, D.T., Luisi, B.F., Miyazaki, G., Perutz, M.F., and Nagai, K.: A mutagenic study of the allosteric linkage of His(HC3) 146 beta in hemoglobin. J. Mol. Biol., 230:1291-6, 1993.