Article
Different pattern of gene mutations in Iranian patients with severe congenital neutropenia (including 2 new mutations).
Iranian journal of allergy, asthma, and immunology - 1 Mar 2013
Alizadeh Zahra, Fazlollahi Mohammad Reza, Houshmand Massoud, Maddah Marzieh, Chavoshzadeh Zahra, Hamidieh Amir Ali, Shamsian Bibi Shahin, Eshghi Payman, Bolandghamat Pour Samaneh, Sadaaie Jahromi Hoda, Mansouri Mahboobeh, Movahedi Masoud, Nayebpour Mohsen, Pourpak Zahra, Moin Mostafa
Abstract excerpt
Severe congenital neutropenia (SCN) is a rare primary immunodeficiency disease. Different genes are found to be associated with SCN, including ELA2, HAX1, WAS, GFI1, G-CSFR and G6PC3. The aim of this study was to find different gene mutations responsible for SCN in Iranian patients. Twenty-seven patients with SCN referred to Immunology, Asthma and Allergy Research Institute during a five year priod 5 years (May...
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