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Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Fondazione Ferrata Storti
2021
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Materias: | |
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 |
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author | 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 |
author_facet | 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 |
author_sort | Marin-Esteban, Viviana |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-8883555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Fondazione Ferrata Storti |
record_format | MEDLINE/PubMed |
spelling | pubmed-88835552022-03-18 Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity 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 Haematologica Letters to the Editor Fondazione Ferrata Storti 2021-12-02 /pmc/articles/PMC8883555/ /pubmed/34854278 http://dx.doi.org/10.3324/haematol.2021.279254 Text en Copyright© 2022 Ferrata Storti Foundation https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Letters to the Editor 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 Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity |
title | Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity |
title_full | Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity |
title_fullStr | Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity |
title_full_unstemmed | Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity |
title_short | Biallelic CXCR2 loss-of-function mutations define a distinct congenital neutropenia entity |
title_sort | biallelic cxcr2 loss-of-function mutations define a distinct congenital neutropenia entity |
topic | Letters to the Editor |
url | 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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