ID   MHHi002-A-1
SY   CF[1]iPS5-corr18b13w3C36
DR   hPSCreg; MHHi002-A-1
DR   Wikidata; Q54905556
RX   PubMed=28925369;
CC   From: Hannover Medical School, LEBAO (MHH); Hannover; Germany.
CC   Characteristics: The homozygous CFTR p.Phe508del (c.1521_1523delCTT) mutation of the donor has been corrected by TALEN.
DI   NCIt; C2975; Cystic fibrosis
OX   NCBI_TaxID=9606; ! Homo sapiens
HI   CVCL_QX52 ! MHHi002-A
SX   Male
CA   Induced pluripotent stem cell
DT   Created: 15-11-17; Last updated: 07-09-18; Version: 3
RX   PubMed=28925369; DOI=10.1016/j.scr.2017.07.010;
RA   Merkert S., Bednarski C., Gohring G., Cathomen T., Martin U.;
RT   "Generation of a gene-corrected isogenic control iPSC line from cystic
RT   fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation
RT   mediated by TALENs and ssODN.";
RL   Stem Cell Res. 23:95-97(2017).