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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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| Publicado no: | Iran Biomed J |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Pasteur Institute
2016
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| 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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