ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY, vol.34, no.1, pp.73-76, 2016 (SCI-Expanded)
Article / Article
ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY
Science Citation Index Expanded (SCI-EXPANDED), Scopus
Severe congenital neutropenia, diagnosis, mutation, HAX-1, ELANE, SEVERE CONGENITAL NEUTROPENIA, MUTATIONS, LEUKEMIA, ELASTASE, ELA2, ABNORMALITIES, DISEASE, G6PC3
Gazi University Affiliated:
Background: Mutations in the HAX-1 gene cause an autosomal recessive form of severe congenital neutropenia (SCN), which particularly manifests with recurrent skin, lung and deep tissue infections from the first few months of life.