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Autor:
Yasuyoshi Tanaka, Norimichi Higurashi, Naoto Shirasu, Shin'ichiro Yasunaga, Kevin Mello Moreira, Hideyuki Okano, Shinichi Hirose
Publikováno v:
Stem Cell Research, Vol 31, Iss , Pp 11-15 (2018)
De novo mutations in SCN1A are the most common cause of Dravet syndrome (DS), an infantile-onset epileptic encephalopathy. In this study, human induced pluripotent stem cell (hiPSC) line FUi002-A was generated from skin fibroblasts obtained from a cl
Externí odkaz:
https://doaj.org/article/a0f2c7162ba54700b42cb8556ca35620