reference/17211368

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17211368

Outgoing Links

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endingPage	1564
issn	0028-3878 1526-632X
issueIdentifier	7
pageRange	1564-1564
publicationName	Neurology
startingPage	1564
bibliographicCitation	Abicht A, Stucka R, Karcagi V, Herczegfalvi A, Horváth R, Mortier W, Schara U, Ramaekers V, Jost W, Brunner J, Janssen G, Seidel U, Schlotter B, Müller-Felber W, Pongratz D, Rüdel R, Lochmüller H. A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin. Neurology. 1999 Oct 22;53(7):1564–9. doi: 10.1212/wnl.53.7.1564. PMID: 10534268.
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date	1999-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1212/wnl.53.7.1564 https://pubmed.ncbi.nlm.nih.gov/10534268
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin
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