Generation of a human iPSC line (UUIGPi015-A) from a patient with Dravet syndrome and a 2.9 Mb deletion spanning SCN1A on chromosome 2
Open Access
- 16 February 2022
- journal article
- research article
- Published by Elsevier in Stem Cell Research
- Vol. 60, 102712
Abstract
No abstract availableKeywords
Funding Information
- Hjärnfonden
- Vetenskapsrådet
This publication has 5 references indexed in Scilit:
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- A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3Parkinsonism & Related Disorders, 2019
- Generation of three human induced pluripotent stem cell (iPSC) lines from three patients with Dravet syndrome carrying distinct SCN1A gene mutationsStem Cell Research, 2019
- A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patientseLife, 2016
- Dravet syndrome—From epileptic encephalopathy to channelopathyEpilepsia, 2014