Hemolytic anemia in the mouse
- 1 March 1983
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Heredity
- Vol. 74 (2) , 88-92
- https://doi.org/10.1093/oxfordjournals.jhered.a109747
Abstract
A new mutation causing spherocytic, hernolytic anemia has been discovered in the house mouse. It is Inherited as a single autosornal recessive gene, allelic with both sph and ha, which, in turn, were shown to be allelic with each other. A revised nomenclature for the three apparent alleles is proposed: sph (formerly sph), sphha (formerly ha), and sph2Bc (the new mutation). Like the other murine hemolytic anemias, sph2Bc involves a defect in the red blood cell membrane protein, spectrin.This publication has 4 references indexed in Scilit:
- Reconstitution of spectrin-deficient, spherocytic mouse erythrocyte membranes.Journal of Clinical Investigation, 1979
- MARKED REDUCTION OF SPECTRIN IN HEREDITARY SPHEROCYTOSIS IN COMMON HOUSE MOUSE1978
- A NEW MUTATION (sph) CAUSING NEONATAL JAUNDICE IN THE HOUSE MOUSECanadian Journal of Genetics and Cytology, 1962
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951