Clinical and Genetic Features in Patients with Cystic Fibrosis in Southwestern Iran

OBJECTIVE: Cystic fibrosis (CF) is a common autosomal recessive genetic disease caused by a mutation in the CF transmembrane conductance regulatory (CFTR) gene. This study attempted to identify the most common CFTR mutations and any correlations between certain mutations and the clinical presentatio...

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Detalles Bibliográficos
Autores principales: Farjadian, Shirin, Moghtaderi, Mozhgan, Kashef, Sara, Alyasin, Soheila, Najib, Khadijehsadat, Saki, Forough
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2013
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3663315/
https://www.ncbi.nlm.nih.gov/pubmed/23724185

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3663315/
https://www.ncbi.nlm.nih.gov/pubmed/23724185

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