Neutrophil dysfunction triggers inflammatory bowel disease in G6PC3 deficiency-Reference-Cited by-同舟云学术

Neutrophil dysfunction triggers inflammatory bowel disease in G6PC3 deficiency

Published:2020-09-15 Issue:6 Volume:109 Page:1147-1154
ISSN:0741-5400
Container-title:Journal of Leukocyte Biology
language:en
Short-container-title:J Leukoc Biol

Author:

Goenka Anu¹²³^ORCID,Doherty John A.¹,Al‐Farsi Tariq²,Jagger Christopher¹,Banka Siddharth⁴⁵,Cheesman Edmund⁶,Fagbemi Andrew⁷,Hughes Stephen M.¹²,Wynn Robert F.⁸,Hussell Tracy¹,Arkwright Peter D¹²

Affiliation:

1. Lydia Becker Institute of Immunology and Inflammation University of Manchester Manchester UK

2. Department of Paediatric Allergy & Immunology Royal Manchester Children's Hospital Manchester UK

3. School of Cellular and Molecular Medicine University of Bristol Bristol UK

4. Division of Evolution and Genomic Sciences Faculty of Biology Medicine and Health University of Manchester Manchester UK

5. Manchester Centre for Genomic Medicine St Mary's Hospital Manchester UK

6. Department of Paediatric Histopathology Royal Manchester Children's Hospital Manchester UK

7. Department of Paediatric Gastroenterology Royal Manchester Children's Hospital Manchester UK

8. Department of Paediatric Haematology Royal Manchester Children's Hospital Manchester UK

Funder

Wellcome Trust

Publisher

Wiley

Subject

Cell Biology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/JLB.5AB1219-699RR

Reference35 articles.

1. The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies

2. Inflammatory Bowel Disease and T cell Lymphopenia in G6PC3 Deficiency

3. Homozygosity Mapping and Whole-Exome Sequencing to Detect SLC45A2 and G6PC3 Mutations in a Single Patient with Oculocutaneous Albinism and Neutropenia

4. Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry

5. Phenotypic Heterogeneity of Neutropenia and Gastrointestinal Illness Associated with G6PC3 Founder Mutation

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