Comprehensive multi-omics analysis of G6PC3 deficiency-related congenital neutropenia with inflammatory bowel disease-Reference-Cited by-同舟云学术

Comprehensive multi-omics analysis of G6PC3 deficiency-related congenital neutropenia with inflammatory bowel disease

Published:2021-03 Issue:3 Volume:24 Page:102214
ISSN:2589-0042
Container-title:iScience
language:en
Short-container-title:iScience

Author:

Dasouki Majed^ORCID,Alaiya Ayodeele^ORCID,ElAmin Tanziel^ORCID,Shinwari Zakia,Monies Dorota,Abouelhoda Mohamed,Jabaan Amjad,Almourfi Feras,Rahbeeni Zuhair^ORCID,Alsohaibani Fahad,Almohareb Fahad,Al-Zahrani Hazzaa,Guzmán Vega Francisco J.,Arold Stefan T.^ORCID,Aljurf Mahmoud^ORCID,Ahmed Syed Osman

Funder

King Abdulaziz City for Science And Technology

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference46 articles.

1. A novel homozygous mutation in G6PC3 presenting as cyclic neutropenia and severe congenital neutropenia in the same family;Alangari;J. Clin. Immunol.,2013

2. G6PC3 deficiency;Banka,2016

3. A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations;Banka;Orphanet J. Rare Dis.,2013

4. Mutations in the G6PC3 gene cause Dursun syndrome;Banka;Am. J. Med. Genet. A,2010

5. Inflammatory bowel disease and T cell lymphopenia in G6PC3 deficiency;Bégin;J. Clin. Immunol.,2012

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