Different Pattern of Gene Mutations in Iranian Patients with Severe Congenital Neutropenia (Including 2 New Mutations)

Different Pattern of Gene Mutations in Iranian Patients with Severe Congenital Neutropenia (Including 2 New Mutations)

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 pa...

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Bibliographic Details
Main Authors: Zahra Alizadeh, Mohammad Reza Fazlollahi, Massoud Houshmand, Marzieh Maddah, Zahra Chavoshzadeh, Amir Ali Hamidieh, Bibi Shahin Shamsian, Payman Eshghi, Samaneh Bolandghamat Pour, Hoda Sadaaie Jahromi, Mahboobeh Mansouri, Masoud Movahedi, Mohsen Nayebpour, Zahra Pourpak, Mostafa Moin
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2013-03-01
Series:Iranian Journal of Allergy, Asthma and Immunology
Subjects:
Neutropenia
Gene mutation
Severe congenital neutropenia
Online Access:https://ijaai.tums.ac.ir/index.php/ijaai/article/view/529

Internet

https://ijaai.tums.ac.ir/index.php/ijaai/article/view/529

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