Analysis of CFTR Gene Mutations in Children with Cystic Fibrosis, First Report from North-East of Iran

Objective(s): More than 1500 registered mutations in cystic fibrosis transmembrane regulator (CFTR) gene are responsible for dysfunction of an ion channel protein and a wide spectrum of clinical manifestations in patients with cystic fibrosis (CF). This study was performed to investigate the frequen...

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Detalles Bibliográficos
Autores principales: Mehdizadeh Hakkak, Atieh, Keramatipour, Mohammad, Talebi, Saeid, Brook, Azam, Tavakol Afshari, Jalil, Raazi, Amin, Kianifar, Hamid Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786104/
https://www.ncbi.nlm.nih.gov/pubmed/24106596

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786104/
https://www.ncbi.nlm.nih.gov/pubmed/24106596

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