Associated Papers
Severe congenital neutropenia due to G6PC3 deficiency: Case series of five patients and literature review.
Velez-Tirado N et al.
Scandinavian Journal of Immunology, 2022
Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population.
López-Rodríguez L et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion, 2022
G6PC3 Deficiency: Primary Immune Deficiency Beyond Just Neutropenia.
Kiykim A et al.
Journal of Pediatric Hematology/oncology, 2015
A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations.
Banka S et al.
Orphanet Journal of Rare Diseases, 2013
Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia.
Boztug K et al.
The Journal of Pediatrics, 2012
Two cases of syndromic neutropenia with a report of novel mutation in G6PC3.
Alizadeh Z et al.
Iranian Journal of Allergy, Asthma, and Immunology, 2011
A case of syndromic neutropenia and mutation in G6PC3.
Gatti S et al.
Journal of Pediatric Hematology/oncology, 2011
Cardiac and renal malformations in a patient with sepsis and severe congenital neutropenia.
Eghbali A et al.
Iranian Journal of Pediatrics, 2010
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