The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell Phenotype
Risinger M, Glogowska E, Begtrup A, Dagaonkar N, Chonat S, Joiner C, Quinn C, Kalfa T, Gallagher P. The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell Phenotype. Blood 2014, 124: 741. DOI: 10.1182/blood.v124.21.741.741.Peer-Reviewed Original ResearchRed blood cellsHereditary hemolytic anemia