reference/30218564

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endingPage	2377
issn	0964-6906 1460-2083
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publicationName	Human Molecular Genetics
startingPage	2370
bibliographicCitation	Blanco-Arias P, Einholm AP, Mamsa H, Concheiro C, Gutiérrez-de-Terán H, Romero J, Toustrup-Jensen MS, Carracedo A, Jen JC, Vilsen B, Sobrido MJ. A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism. Hum Mol Genet. 2009 Jul 01;18(13):2370–7. doi: 10.1093/hmg/ddp170. PMID: 19351654.
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date	2009-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1093/hmg/ddp170 https://pubmed.ncbi.nlm.nih.gov/19351654
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism
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