CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation
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Title
CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation
Authors
Keywords
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Journal
Translational Psychiatry
Volume 6, Issue 1, Pages e703-e703
Publisher
Springer Nature
Online
2016-01-05
DOI
10.1038/tp.2015.203
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