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Brain. 2016 Aug;139(Pt 8):e46. doi: 10.1093/brain/aww115. Epub 2016 May 19.

Multisystemic SYNE1 ataxia: confirming the high frequency and extending the mutational and phenotypic spectrum.

Author information

1
1 Neurogenetics Group, Department of Molecular Genetics, VIB, Antwerpen, Belgium 2 Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Belgium.
2
3 Institute of Medical Genetics and Applied Genomics, University of Tübingen, Germany.
3
4 Department of Neurology, University Hospital of Bonn, Germany 5 German Research Centre for Neurodegenerative Diseases (DZNE), Bonn, Germany.
4
6 Department of Neurology, University of Duisburg-Essen, Essen, Germany.
5
7 Unit of Genetics of Neurodegenerative and Metabolic Diseases, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
6
8 Department of Neurology, Gumussuyu Military Hospital, Istanbul, Turkey.
7
9 Division of Neurology, Department of Neuroscience, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
8
10 Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Germany 11 German Research Centre for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
9
12 Dr John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, USA.
10
1 Neurogenetics Group, Department of Molecular Genetics, VIB, Antwerpen, Belgium 2 Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Belgium 13 Department of Neurology, Antwerp University Hospital, Belgium.
11
10 Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen, Germany 11 German Research Centre for Neurodegenerative Diseases (DZNE), Tübingen, Germany matthis.synofzik@uni-tuebingen.de.
PMID:
27197992
PMCID:
PMC4958896
DOI:
10.1093/brain/aww115
[Indexed for MEDLINE]
Free PMC Article

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