reference/25126652

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25126652

Outgoing Links

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endingPage	e104
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pageRange	e104-e104
publicationName	Journal of Medical Genetics
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bibliographicCitation	Müller JS, Abicht A, Burke G, Cossins J, Richard P, Baumeister SK, Stucka R, Eymard B, Hantaï D, Beeson D, Lochmüller H. The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder. J Med Genet. 2004 Aug;41(8):e104. PMID: 15286164; PMCID: PMC1735862.
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date	2004-08-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1136/jmg.2004.021139 https://pubmed.ncbi.nlm.nih.gov/PMC1735862 https://pubmed.ncbi.nlm.nih.gov/15286164
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder
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Incoming Links

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Total number of triples: 50.