Mutation Analysis of Exons 10 and 17a of CFTR Gene in Patients with Cystic Fibrosis in Kermanshah Province, Western Iran

BACKGROUND: Cystic fibrosis (CF) is the most common genetic disorder with autosomal recessive inheritance among Caucasian populations. So far, more than 1950 different mutations were identified in cystic fibrosis transmembrane conductance regulator (CFTR) gene. CFTR gene has 27 exons. The type and d...

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Detalles Bibliográficos
Autores principales: Sahami, Abbas, Alibakhshi, Reza, Ghadiri, Keyghobad, Sadeghi, Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2014
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955424/
https://www.ncbi.nlm.nih.gov/pubmed/24696795

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955424/
https://www.ncbi.nlm.nih.gov/pubmed/24696795

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