@article{oai:nagasaki-u.repo.nii.ac.jp:00002028,
 author = {Yamamoto, Takuma and Otsu, Makoto and Okumura, Takashi and Horie, Yumi and Ueno, Yasuharu and Taniguchi, Hideki and Ohtaka, Manami and Nakanishi, Mahito and Abe, Yuki and Murase, Takehiko and Umehara, Takahiro and Ikematsu, Kazuya},
 journal = {Stem Cell Research},
 month = {Jun},
 note = {We established three iPSC lines from postmortem-cultured fibroblasts derived following the sudden unexpected death of an 8-year-old girl with Lennox-Gastaut syndrome,
 who turned out to have the R551H-mutant STXBP1 gene. These iPSC clones showed pluripotent characteristics while retaining the genotype and demonstrated trilineage differentiation capability, indicating their utility in disease-modeling studies, i.e., STXBP1-encephalopathy. This is the first report on the establishment of iPSCs from a sudden death child, suggesting the possible use of postmortem-iPSC technologies as an epoch-making approach for precise identification of the cause of sudden death., Stem Cell Research, 39, art.no.101485; 2019},
 title = {Generation of three induced pluripotent stem cell lines from postmortem tissue derived following sudden death of a young patient with STXBP1 mutation},
 volume = {39},
 year = {2019}
}