Open AccessBiallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity
Author(s) -
Viviana MarinEsteban,
Jenny Youn,
Blandine Beaupain,
Agnieszka JaraczRos,
Vincent Barlogis,
Odile Fenneteau,
Thierry Leblanc,
Florence Bellanger,
Philippe Pellet,
Julien Buratti,
Hélène Lapillonne,
Françoise Bachelerie,
Jean Donadieu,
Christine BellannéChantelot
Publication year - 2021
Publication title -
haematologica
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.782
H-Index - 142
eISSN - 1592-8721
pISSN - 0390-6078
DOI - 10.3324/haematol.2021.279254
Subject(s) - congenital neutropenia , neutropenia , loss function , gain of function , function (biology) , medicine , mutation , genetics , biology , phenotype , gene , chemotherapy
Not available.