Suggestions

Du même auteur

Incidence of ATRX mutations in myelodysplastic syndromes, the value of micr...

Archive ouverte: Article de revue

Herbaux, Charles | 2015-08

International audience. Acquired α-thalassemia myelodysplastic syndrome (MDS) (ATMDS) is an acquired syndrome characterized by a somatic point mutation or splicing defect in the ATRX gene in patients with myeloid di...

PIEZO1 activation delays erythroid differentiation of normal and hereditary...

Archive ouverte: Article de revue

Caulier, Alexis | 2020

International audience. Hereditary xerocytosis is a dominantly inherited red cell membrane disorder caused in most cases by gain-of-function mutations in PIEZO1, encoding a mechanosensitive ion channel that translat...

Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardo...

Archive ouverte: Article de revue

Picard, Veronique | 2019

International audience. We describe the clinical, hematologic and genetic characteristics of a retrospective series of 126 subjects from 64 families with hereditary xerocytosis. Twelve patients from six families car...

Chargement des enrichissements...