Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity - Sorbonne Université
Journal Articles Haematologica Year : 2021

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

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Hematology
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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

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hal-03465048 , version 1 (03-12-2021)

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Viviana Marin-Esteban, Jenny Youn, Blandine Beaupain, Agnieszka Jaracz-Ros, Vincent Barlogis, et al.. Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity. Haematologica, In press, ⟨10.3324/haematol.2021.279254⟩. ⟨hal-03465048⟩

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INSERM FNCLCC IGR U938 UNIV-PARIS-SACLAY SORBONNE-UNIVERSITE SU-MEDECINE GS-LIFE-SCIENCES-HEALTH GS-HEALTH-DRUG-SCIENCES CSHMYELO MI2
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