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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Farjadian, Shirin, Moghtaderi, Mozhgan, Kashef, Sara, Alyasin, Soheila, Najib, Khadijehsadat, Saki, Forough
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Tehran University of Medical Sciences 2013
Aiheet:
Short Communication
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3663315/
https://ncbi.nlm.nih.gov/pubmed/23724185
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