reference/2706203

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2706203

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bibliographicCitation	Pfeffer G, Pyle A, Griffin H, Miller J, Wilson V, Turnbull L, Fawcett K, Sims D, Eglon G, Hadjivassiliou M, Horvath R, Németh A, Chinnery PF. SPG7 mutations are a common cause of undiagnosed ataxia. Neurology. 2015 Mar 17;84(11):1174–6. doi: 10.1212/wnl.0000000000001369.
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date	2015-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1212/wnl.0000000000001369 https://pubmed.ncbi.nlm.nih.gov/25681447 https://pubmed.ncbi.nlm.nih.gov/PMC4371411
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	SPG7 mutations are a common cause of undiagnosed ataxia
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Total number of triples: 64.