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Cellular and molecular life sciences : CMLS, 2015-09, Vol.72 (17), p.3387-3399
2015
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PLoS genetics, 2015-03, Vol.11 (3), p.e1005021-e1005021
2015
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Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia
- Nibbeling, Esther A R
- Duarri, Anna
- Verschuuren-Bemelmans, Corien C
- Fokkens, Michiel R
- Karjalainen, Juha M
- Smeets, Cleo J L M
- de Boer-Bergsma, Jelkje J
- van der Vries, Gerben
- Dooijes, Dennis
- Bampi, Giovana B
- van Diemen, Cleo
- Brunt, Ewout
- Ippel, Elly
- Kremer, Berry
- Vlak, Monique
- Adir, Noam
- Wijmenga, Cisca
- van de Warrenburg, Bart P C
- Franke, Lude
- Sinke, Richard J
- Verbeek, Dineke S
2017
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Proceedings of the National Academy of Sciences - PNAS, 2022-08, Vol.119 (34), p.e2208513119-e2208513119
2022
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Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23
2021
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Brain (London, England : 1878), 2016-08, Vol.139 (Pt 8), p.e43-e43
2016
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Brain (London, England : 1878), 2015-09, Vol.138 (Pt 9), p.2537-2552
2015
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Human molecular genetics, 2016-07, Vol.25 (13), p.2728
2016
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- Spinocerebellar Degenerations - Genetics
- Clinical Neurology
- Mice, Transgenic
- Neurodegeneration
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- Spinocerebellar Ataxia
- Ataxia
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- Cerebellum - Pathology
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- Brain
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- Cellular And Molecular Life Sciences
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- Human Molecular Genetics
- Human Molecular Genetics Online/human Molecular Genetics
- Plos Genetics
- Proceedings Of The National Academy Of Sciences - Pnas
- Proceedings Of The National Academy Of Sciences Of The United States Of America