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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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Detalles Bibliográficos
Autores principales: Abdul-Qadir, Asal Gailan, Al-Musawi, Bassam Musa, Thejeal, Rabab Farhan, Al-Omar, Saad Abdul-Baqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110311/
http://dx.doi.org/10.1186/s43042-021-00164-x