Mutations in the G6PC3 gene cause Dursun syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference10 articles.
1. A novel G6PC3 homozygous 1-bp deletion as a cause of severe congenital neutropenia;Arostegui;Blood,2009
2. Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3;Banka;Eur J Hum Genet
3. A syndrome with congenital neutropenia and mutations in G6PC3;Boztug;New Engl J Med,2009
4. Familial pulmonary arterial hypertension, leucopenia, and atrial septal defect: A probable new familial syndrome with multisystem involvement;Dursun;Clin Dysmorphol,2009
5. Digenic mutations in severe congenital neutropenia;Germeshausen;Haematologica,2010
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1. Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype of a patient;Allergy, Asthma & Clinical Immunology;2023-06-09
2. Severe congenital neutropenia type 4 with early-onset inflammatory bowel disease attributed to a G6PC3 variant (not previously associated with disease): A case report and a literature review;Human Gene;2023-05
3. Historical Cohort of Severe Congenital Neutropenia in Iran: Clinical Course, Laboratory Evaluation, Treatment, and Survival;Journal of Pediatric Hematology/Oncology;2023-04-10
4. Neutropenia congénita de tipo IV: reporte de un caso;Archivos Argentinos de Pediatria;2022-10-01
5. ASSESSMENT OF CONGENITAL NEUTROPENIA IN CHILDREN: COMMON CLINICAL SCENERIES AND CLUES FOR MANAGEMENT;Mediterranean Journal of Hematology and Infectious Diseases;2022-01-01
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