Genetic modification of cystic fibrosis with ΔF508 mutation of CFTR gene using the CRISPR system in peripheral blood mononuclear cells

Objective(s): Cystic fibrosis (CF) is an inherited autosomal recessive disease that is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The present study aimed to investigate the genetic modification of CF with ΔF508 mutation of the CFTR gene using CRISPR i...

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Detaylı Bibliyografya
Asıl Yazarlar:	Sepideh Khatibi, Mohammad Reza Modaresi, Reza Kazemi Oskuee, Mohammad Salehi, Hamid Aghaei
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	Mashhad University of Medical Sciences 2021-01-01
Seri Bilgileri:	Iranian Journal of Basic Medical Sciences
Konular:	cftr gene crispr cystic fibrosis peripheral blood mononuclear cells δf508 mutation
Online Erişim:	https://ijbms.mums.ac.ir/article_17031_41e69d647dcaba0322ebd32eea51c085.pdf
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Genetic modification of cystic fibrosis with ΔF508 mutation of CFTR gene using the CRISPR system in peripheral blood mononuclear cells

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