reference/12073013

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12073013

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endingPage	10
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pageRange	1305-10
publicationName	JAMA Neurology
startingPage	1305
bibliographicCitation	Renaud M, Anheim M, Kamsteeg EJ, Mallaret M, Mochel F, Vermeer S, Drouot N, Pouget J, Redin C, Salort-Campana E, Kremer HP, Verschuuren-Bemelmans CC, Muller J, Scheffer H, Durr A, Tranchant C, Koenig M. Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study. JAMA Neurol. 2014 Oct;71(10):1305–10. doi: 10.1001/jamaneurol.2014.193. PMID: 25089919.
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date	2014-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/25089919 https://doi.org/10.1001/jamaneurol.2014.193
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study
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