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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mohseni, Marzieh, Razzaghmanesh, Mohammad, Mehr, Elham Parsi, Zare, Hanieh, Beheshtian, Maryam, Najmabadi, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute 2016
Materias:
Full Length
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983674/
https://www.ncbi.nlm.nih.gov/pubmed/27017198
http://dx.doi.org/10.7508/ibj.2016.04.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983674/
https://www.ncbi.nlm.nih.gov/pubmed/27017198
http://dx.doi.org/10.7508/ibj.2016.04.003

Ejemplares similares