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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Pasteur Institute
2016
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| Materias: | |
| 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 |