Related references
Note: Only part of the references are listed.Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis
Edyta Glogowska et al.
BLOOD (2015)
A mutation in the Gardos channel is associated with hereditary xerocytosis
Raphael Rapetti-Mauss et al.
BLOOD (2015)
Hereditary xerocytosis revisited
Natasha M. Archer et al.
AMERICAN JOURNAL OF HEMATOLOGY (2014)
Slower Piezo1 Inactivation in Dehydrated Hereditary Stomatocytosis (Xerocytosis)
Sophie Demolombe et al.
BIOPHYSICAL JOURNAL (2013)
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
Immacolata Andolfo et al.
BLOOD (2013)
Iron overload in a teenager with xerocytosis: the importance of nuclear magnetic resonance imaging
Reijane Alves de Assis et al.
EINSTEIN-SAO PAULO (2013)
Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis
Ryan Zarychanski et al.
BLOOD (2012)
Clinicopathological study of Japanese patients with genetic iron overload syndromes
Ai Hattori et al.
PATHOLOGY INTERNATIONAL (2012)
Bulky extramedullary hematopoiesis is not a rare complication of congenital dyserythropoietic anemia
Hermann Heimpel et al.
ANNALS OF HEMATOLOGY (2009)
Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis
P. -Y. Syfuss et al.
CLINICAL AND LABORATORY HAEMATOLOGY (2006)
The role of HFE mutations on iron metabolism in beta-thalassemia carriers
R Martins et al.
JOURNAL OF HUMAN GENETICS (2004)
Dehydrated hereditary stomatocytosis with transient perinatal ascites
AP Basu et al.
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION (2003)
Share Paper
