reference/36296588

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/36296588

Outgoing Links

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contentType	Journal Article
issn	0920-1211
pageRange	107266-
publicationName	Epilepsy Research
startingPage	107266
bibliographicCitation	Sierra-Marcos A, Ribosa-Nogué R, Vidal-Robau N, Aldecoa I, Turón E, Rodríguez-Santiago B, Turón M, Boronat S, Molina-Porcel L. Inherited SCN1A missense mutation in a Dravet Syndrome family: Neuropathological correlation, family screening and implications for adult carriers. Epilepsy Res. 2024 Jan;199():107266. doi: 10.1016/j.eplepsyres.2023.107266. PMID: 38061235.
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date	202401
identifier	https://doi.org/10.1016/j.eplepsyres.2023.107266 https://pubmed.ncbi.nlm.nih.gov/38061235
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Inherited SCN1A missense mutation in a Dravet Syndrome family: Neuropathological correlation, family screening and implications for adult carriers
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Incoming Links

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Total number of triples: 38.