Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity.
Marin-Esteban V, Youn J, Beaupain B, Jaracz-Ros A, Barlogis V, Fenneteau O, Leblanc T, Bellanger F, Pellet P, Buratti J, Lapillonne H, Bachelerie F, Donadieu J, Bellanné-Chantelot C.
Marin-Esteban V, et al. Among authors: jaracz ros a.
Haematologica. 2022 Mar 1;107(3):765-769. doi: 10.3324/haematol.2021.279254.
Haematologica. 2022.
PMID: 34854278
Free PMC article.
No abstract available.