Hemoglobin casper: β 106 (G8) Leu→Pro: A contemporary mutation
- 31 October 1973
- journal article
- research article
- Published by Elsevier in American Journal Of Medicine
- Vol. 55 (4), 549-558
- https://doi.org/10.1016/0002-9343(73)90213-1
Abstract
No abstract availableKeywords
This publication has 78 references indexed in Scilit:
- Hemoglobin Savannah (B6(24) β-glycine→valine): an unstable variant causing anemia with inclusion bodiesJCI Insight, 1971
- Two new pathological haemoglobins: Olmsted β141 (H19) Leu → to Arg and Malmö β97 (FG4) His → to GlnBiochemical Journal, 1970
- Idiopathic Heinz Body Anaemia: Hb‐Bristol (β67 (E11) Val→Asp)British Journal of Haematology, 1970
- Subunit Dissociation of the Unstable Hemoglobin Bibba (α2136 ro (H19)β2)Published by Elsevier ,1970
- In vitro Synthesis of Hb Hammersmith (CD1 Phe→Ser)Nature, 1970
- Congenital Heinz-body haemolytic anaemia due to haemoglobin HammersmithPublished by Oxford University Press (OUP) ,1969
- Three families with unstable hemoglobinopathies (Köln, Olmsted and Santa Ana) causing hemolytic anemia with inclusion bodies and pigmenturiaAmerican Journal Of Medicine, 1969
- HemoglobinBibba or α2136Proβ2, an unstable α chain abnormal hemoglobinBiochimica et Biophysica Acta (BBA) - Protein Structure, 1968
- Haemoglobin Hammersmith (β 42 (CD1) Phe→Ser)Nature, 1967
- Congenital Heinz‐Body AnaemiaBritish Journal of Haematology, 1964