Haemoglobin Hallamshire (β146 HIS → TYR): A new high oxygen affinity haemoglobin responsible for familial erythrocytosis

Clinical and Laboratory Haematology

Volumn 18, Issue 4, 1996, Pages 237-239

  Leach, M ^a   Greaves, M ^b   Porter, N ^a   Williamson, D ^c   Brown, K ^d  

^a ROYAL HALLAMSHIRE HOSPITAL   (United Kingdom)

^b ABERDEEN ROYAL INFIRMARY   (United Kingdom)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^d CAMBRIDGE UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

Familial erythrocytosis; Haemoglobin oxygen affinity; Hb variants

Indexed keywords

HEMOGLOBIN VARIANT; HISTIDINE; OXYHEMOGLOBIN; TYROSINE;

ADULT; ARTICLE; CASE REPORT; ERYTHROCYTOSIS; GENE MUTATION; HUMAN; HUMAN CELL; MALE; OXYGEN AFFINITY; PRIORITY JOURNAL; BLOOD; FAMILY HEALTH; FEMALE; GENETICS; HETEROZYGOTE; METABOLISM; PATHOPHYSIOLOGY; PH; PHYSIOLOGY; POINT MUTATION; POLYCYTHEMIA; PROTEIN ELECTROPHORESIS;

ADULT; BLOOD PROTEIN ELECTROPHORESIS; FAMILY HEALTH; FEMALE; HEMOGLOBINS, ABNORMAL; HETEROZYGOTE; HISTIDINE; HUMANS; HYDROGEN-ION CONCENTRATION; MALE; OXYHEMOGLOBINS; POINT MUTATION; POLYCYTHEMIA; TYROSINE;

EID: 0030300179     PISSN: 01419854     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

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