reference/32220900

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/32220900

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, N.I.H., Extramural\|Research Support, Non-U.S. Gov't
endingPage	20
issn	0014-3022 1421-9913
issueIdentifier	1
pageRange	16-20
publicationName	European Neurology
startingPage	16
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bibliographicCitation	Marti S, Baloh RW, Jen JC, Straumann D, Jung HH. Progressive cerebellar ataxia with variable episodic symptoms--phenotypic diversity of R1668W CACNA1A mutation. Eur Neurol. 2008;60(1):16–20. doi: 10.1159/000127974. PMID: 18437043.
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date	2008
identifier	https://doi.org/10.1159/000127974 https://pubmed.ncbi.nlm.nih.gov/18437043
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Progressive Cerebellar Ataxia with Variable Episodic Symptoms – Phenotypic Diversity of R1668W CACNA1A Mutation
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Total number of triples: 52.