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Isogenic Cell Models of Cystic Fibrosis-Causing Variants in Natively Expressing Pulmonary Epithelial Cells.

Journal of Cystic Fibrosis(2018)

Cited 90|Views34
Key words
Cystic Fibrosis,CFTR,Model system,CRISPR/Cas9,Premature termination codon,Nonsense mutation
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