Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity
Domains
HematologyOrigin | Publication funded by an institution |
---|
_ |
Origin | Publication funded by an institution |
---|
Gestionnaire HAL 4 Sorbonne Université : Connect in order to contact the contributor
https://hal.sorbonne-universite.fr/hal-03465048
Submitted on : Friday, December 3, 2021-3:52:01 PM
Last modification on : Monday, October 14, 2024-3:02:03 PM
Long-term archiving on : Friday, March 4, 2022-7:18:44 PM