reference/30288757

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30288757

Outgoing Links

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contentType	Case Reports\|Journal Article
endingPage	364
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issueIdentifier	2
pageRange	362-364
publicationName	The Journal of Pediatrics
startingPage	362
bibliographicCitation	LaPage MJ, Russell MW, Bradley DJ, Dick M. Novel Ryanodine Receptor 2 Mutation Associated with a Severe Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia. The Journal of Pediatrics. 2012 Aug;161(2):362–4. doi: 10.1016/j.jpeds.2012.04.013.
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date	201208
identifier	https://pubmed.ncbi.nlm.nih.gov/22608700 https://doi.org/10.1016/j.jpeds.2012.04.013
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Novel Ryanodine Receptor 2 Mutation Associated with a Severe Phenotype of Catecholaminergic Polymorphic Ventricular Tachycardia
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Total number of triples: 42.