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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Origin Publication funded by an institution

Dates and versions

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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