reference/16835990

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16835990

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
endingPage	39
issn	0920-1211
pageRange	34-39
publicationName	Epilepsy Research
startingPage	34
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bibliographicCitation	Lim BC, Hwang H, Kim H, Chae JH, Choi J, Kim KJ, Hwang YS, Yum MS, Ko TS. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome? Epilepsy Res. 2015 Jan;109():34–9. doi: 10.1016/j.eplepsyres.2014.10.008. PMID: 25524840.
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date	201501
identifier	https://doi.org/10.1016/j.eplepsyres.2014.10.008 https://pubmed.ncbi.nlm.nih.gov/25524840
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
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Total number of triples: 64.