reference/22325273

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22325273

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contentType	Journal Article
issn	1422-0067
issueIdentifier	10
pageRange	3113-
publicationName	International Journal of Molecular Sciences
startingPage	3113
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bibliographicCitation	Maksemous N, Smith RA, Sutherland HG, Sampaio H, Griffiths LR. Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity. Int J Mol Sci. 2018 Oct 11;19(10). PMID: 30314295; PMCID: PMC6213185.
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date	2018-10-11^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/30314295 https://pubmed.ncbi.nlm.nih.gov/PMC6213185 https://doi.org/10.3390/ijms19103113
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity
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