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

Detalles Bibliográficos
Autores principales: Marin-Esteban, Viviana, Youn, Jenny, Beaupain, Blandine, Jaracz-Ros, Agnieszka, Barlogis, Vincent, Fenneteau, Odile, Leblanc, Thierry, Bellanger, Florence, Pellet, Philippe, Buratti, Julien, Lapillonne, Hélène, Bachelerie, Françoise, Donadieu, Jean, Bellanné-Chantelot, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2021
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8883555/
https://www.ncbi.nlm.nih.gov/pubmed/34854278
http://dx.doi.org/10.3324/haematol.2021.279254

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8883555/
https://www.ncbi.nlm.nih.gov/pubmed/34854278
http://dx.doi.org/10.3324/haematol.2021.279254

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