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Molecular analysis of CFTR gene mutations among Iraqi cystic fibrosis patients
BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive multisystem disease that results from mutation(s) of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. More than 2100 mutations and polymorphisms have been reported in this gene so far. Incidence and genotyping of CF are u...
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| Publicado no: | Egypt J Med Hum Genet |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8110311/ https://ncbi.nlm.nih.gov/pubmed/38624701 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s43042-021-00164-x |
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