Conboy, J. G., Chasis, J. A., Winardi, R., Tchernia, G., Kan, Y. W., & Mohandas, N. (1993). An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.

Conboy, J G., J A. Chasis, R. Winardi, G. Tchernia, Y W. Kan, and N. Mohandas. An Isoform-specific Mutation in the Protein 4.1 Gene Results in Hereditary Elliptocytosis and Complete Deficiency of Protein 4.1 in Erythrocytes but Not in Nonerythroid Cells. 1993.

Conboy, J G., et al. An Isoform-specific Mutation in the Protein 4.1 Gene Results in Hereditary Elliptocytosis and Complete Deficiency of Protein 4.1 in Erythrocytes but Not in Nonerythroid Cells. 1993.