Frequency of Genotype With ΔF508 Mutation in CFTR Gene Among Iranian Cystic Fibrosis Patients With Pancreatic Insufficiency

BACKGROUND: Cystic fibrosis (CF) is the most prevalent lethal autosomal recessive disease with a broad spectrum of phenotypes. Mutation of ΔF508 in the CFTR gene is the most important and lethal mutation in CF, which contains 70% of all predisposing mutations for CF worldwide. OBJECTIVES: Determinin...

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Detalles Bibliográficos
Autores principales: Khodadad, Ahmad, Elahi, Elaheh, Bani Hassani, Setareh Sadat, Rouhani, Pejman, Sadeghi, Bamdad, Rezaei, Nima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2015
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4662842/
https://www.ncbi.nlm.nih.gov/pubmed/26635942
http://dx.doi.org/10.5812/ijp.3419

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