Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome.

Hiroshi Maeda,Tomohiro Chiyonobu,Michiko Yoshida,Satoshi Yamashita,Masashi Zuiki,Satoshi Kidowaki,Kenichi Isoda,Kazuhiro Yamakawa,Masafumi Morimoto,Tatsutoshi Nakahata,Megumu K. Saito,Hajime Hosoi

Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome.

2016

Hiroshi Maeda
Tomohiro Chiyonobu
Michiko Yoshida
Satoshi Yamashita
Masashi Zuiki
Satoshi Kidowaki
Kenichi Isoda
Kazuhiro Yamakawa
Masafumi Morimoto
Tatsutoshi Nakahata
Megumu K. Saito
Hajime Hosoi

Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome

Keywords:

Genetics
Molecular biology
Dravet syndrome
Genetic epidemiology
Medical genetics
Human genetics
Cytogenetics
Statistical genetics
Neurocognitive
Biology
Mutation
Induced pluripotent stem cell
Tyrosine hydroxylase
Molecular genetics
Epigenetics
Mutant
Phenotype

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