Reappraisal of Frequency of Common Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations in Iranian Cystic Fibrosis Patients

BACKGROUND: Cystic Fibrosis (CF) is a life-threatening recessive genetic disorder resulting from mutations in the gene encoding the fibrosis transmembrane conductance regulator protein (CFTR). The CF clinical phenotype shows wide variation ranging from severe disease in early childhood in those homo...

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Detalles Bibliográficos
Autores principales: Khalilzadeh, Soheila, Hassanzad, Maryam, PourAbdollah Toutkaboni, Mihan, Tashayoie Nejad, Sabereh, Sheikholeslami, Fatemeh-Maryam, Velayati, Ali Akbar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Research Institute of Tuberculosis and Lung Disease 2018
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Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320558/
https://www.ncbi.nlm.nih.gov/pubmed/30627177

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