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Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis

BACKGROUND: Cystic fibrosis (CF) is a common autosomal recessive disorder that affects many body systems and is produced by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CF is also the most frequently inherited disorder in the West. The aim of this study was to de...

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Detalhes bibliográficos
Publicado no:Iran Biomed J
Main Authors: Mohseni, Marzieh, Razzaghmanesh, Mohammad, Mehr, Elham Parsi, Zare, Hanieh, Beheshtian, Maryam, Najmabadi, Hossein
Formato: Artigo
Idioma:Inglês
Publicado em: Pasteur Institute 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4983674/
https://ncbi.nlm.nih.gov/pubmed/27017198
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7508/ibj.2016.04.003
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