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- W2136385218 endingPage "396" @default.
- W2136385218 startingPage "385" @default.
- W2136385218 abstract "Primary immunodeficiency diseases (PID) comprise a heterogeneous group of inherited diseases with a wide spectrum of clinical manifestations and laboratory abnormalities. Definite diagnosis of a PID is performed most reliably by detection of a gene mutation which will allow genetic counseling. In addition, detection and confirmation of PIDs that were not severe enough during childhood to lead to a specific diagnosis would be possible. As a definite diagnosis of PID is of importance for the management of these disorders, we present a review on studies that have investigated mutations among patients with different types of PID in Iran. Although the frequency of a definite molecular diagnosis of PID in Iran is acceptable in a developing country, we believe that providing additional laboratory resources and diagnostic methods, development of specialized centers for PID, in addition to improvement of physicians' awareness, may facilitate clinical and genetic diagnosis of patients with PID in Iran." @default.
- W2136385218 created "2016-06-24" @default.
- W2136385218 creator A5008915149 @default.
- W2136385218 creator A5051258190 @default.
- W2136385218 creator A5058600270 @default.
- W2136385218 creator A5091447901 @default.
- W2136385218 date "2014-01-22" @default.
- W2136385218 modified "2023-10-02" @default.
- W2136385218 title "Molecular diagnosis of primary immunodeficiency diseases in a developing country: Iran as an example" @default.
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