Derivation of iPSC line (RCMGi002-A) from dermal fibroblasts of a cystic fibrosis female patient with homozygous F508del mutation.
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DOI: 10.1016/j.scr.2021.102251
Abstract: Cystic fibrosis is one of the most common inherited diseases caused by mutations in CFTR gene, of which F508del is the most frequent. Currently, the possibility of cell therapy including genome editing is widely discussed.… read more here.
Keywords: cystic fibrosis; fibrosis; derivation ipsc; line rcmgi002 ... See more keywords