reference/22214498

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publicationName	European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
startingPage	72
bibliographicCitation	Kinder S, Ossig C, Wienecke M, Beyer A, von der Hagen M, Storch A, Smitka M. Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine. European Journal of Paediatric Neurology. 2015 Jan;19(1):72–4. doi: 10.1016/j.ejpn.2014.10.005.
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date	201501
identifier	https://doi.org/10.1016/j.ejpn.2014.10.005 https://pubmed.ncbi.nlm.nih.gov/25468264
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine
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