Macerollo, A; Mencacci, NE; Erro, R; Cordivari, C; Edwards, MJ; Wood, NW; Bhatia, KP (2014) Screening of mutations in NOL3 in a myoclonic syndromes series. J Neurol, 261 (9). pp. 1830-1831. ISSN 1432-1459 https://doi.org/10.1007/s00415-014-7463-z
SGUL Authors: Edwards, Mark John James

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Item Type:	Article
Additional Information:	© The Author(s) 2014 Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
Keywords:	Aged, Apoptosis Regulatory Proteins, Cerebral Cortex, Electroencephalography, Female, Genetic Testing, Humans, Male, Middle Aged, Muscle Proteins, Mutation, Missense, Myoclonus, Phenotype, Syndrome, Cerebral Cortex, Humans, Myoclonus, Syndrome, Muscle Proteins, Electroencephalography, Phenotype, Mutation, Missense, Aged, Middle Aged, Female, Male, Apoptosis Regulatory Proteins, Genetic Testing, Neurology & Neurosurgery, 1103 Clinical Sciences, 1109 Neurosciences
SGUL Research Institute / Research Centre:	Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Neuroscience (INCCNS)
Journal or Publication Title:	J Neurol
ISSN:	1432-1459
Language:	eng
Dates:	Date Event September 2014 Published 20 August 2014 Published Online 5 August 2014 Accepted
Publisher License:	Creative Commons: Attribution 4.0
PubMed ID:	25138476
Web of Science ID:	WOS:000341791300027
	Go to PubMed abstract
URI:	https://openaccess.sgul.ac.uk/id/eprint/109518
Publisher's version:	https://doi.org/10.1007/s00415-014-7463-z

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