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.

Por Conboy, J G, Chasis, J A, Winardi, R, Tchernia, G, Kan, Y W, Mohandas, N
Publicado em 1993

Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3.

Por Mohandas, N, Winardi, R, Knowles, D, Leung, A, Parra, M, George, E, Conboy, J, Chasis, J
Publicado em 1992