The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene
- 1 September 1992
- journal article
- research article
- Published by Springer Nature in Nature Genetics
- Vol. 2 (1) , 80-83
- https://doi.org/10.1038/ng0992-80
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mochaBlood, 1991
- Organization of the gene for human erythrocyte membrane protein 4.2: structural similarities with the gene for the a subunit of factor XIII.Proceedings of the National Academy of Sciences, 1991
- Primary structure of keratinocyte transglutaminase.Proceedings of the National Academy of Sciences, 1990
- Spectrin-based membrane skeleton: a multipotential adaptor between plasma membrane and cytoplasmPhysiological Reviews, 1990
- Molecular cloning of human protein 4.2: a major component of the erythrocyte membrane.Proceedings of the National Academy of Sciences, 1990
- Complete amino acid sequence and homologies of human erythrocyte membrane protein band 4.2.Proceedings of the National Academy of Sciences, 1990
- Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane.Journal of Clinical Investigation, 1988
- Immature dense granules in platelets from mice with platelet storage pool diseaseBlood, 1987
- Platelet storage pool deficiency in mouse pigment mutations associated with seven distinct genetic lociBlood, 1984
- Ultrastructure of developing melanosomes in C57 Black and pallid miceDevelopmental Biology, 1970