Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity

Haematologica. 2021 Dec 2. doi: 10.3324/haematol.2021.279254. Online ahead of print.ABSTRACTNot available.PMID:34854278 | DOI:10.3324/haematol.2021.279254

Source: Haematologica - December 2, 2021 Category: Hematology Authors: Viviana Marin-Esteban Jenny Youn Blandine Beaupain Agnieszka Jaracz-Ros Vincent Barlogis Odile Fenneteau Thierry Leblanc Florence Bellanger Philippe Pellet Julien Buratti H élène Lapillonne Fran çoise Bachelerie Jean Donadieu Christine Bellann é-Chant Source Type: research