Showing 1 - 1 results of 1 for search 'Fakhrossadat Mortazavi', query time: 0.02s
Refine Results
-
1
Prevalence of the MEFV gene mutations and their clinical correlations in Azeri Turkish patients with childhood Henoch-Schonlein purpura: The role of M680I and E148Q mutations by Mandana Rafeey, Morteza Jabbarpour-Bonyadi, Behzad Aliyari, Mahnaz Sadeghi-Shabestari, Fakhrossadat Mortazavi
Published 2015-06-01
Article