Molecular analysis of exon 13 of cystic fibrosis patients in Middle East: High frequency of K710X mutation
Author:
Funder
Kermanshah University of Medical Sciences in Iran
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference38 articles.
1. Heterogeneity of the cystic fibrosis phenotype in a large kindred family in Qatar with cystic fibrosis mutation (I1234V);Abdul;J. Trop. Pediatr.,2001
2. A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population;Akhavan-Niaki;Blood Cell Mol. Dis.,2011
3. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations;Alibakhshi;J. Cyst. Fibros.,2008
4. Mutation analysis of PAH gene in patients with PKU in western Iran and its association with polymorphisms: identification of four novel mutations;Alibakhshi;Metab. Brain Dis.,2014
5. Novel mutation in the CFTR gene of cystic fibrosis patients in Oman;Al-Kindy;Journal of Molecular Biomarkers & Diagnosis.,2014
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