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  Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only

Wilcox, R., Brænne, I., Brüggemann, N., Winkler, S., Wiegers, K., Bertram, L., et al. (2015). Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only. Journal of Neurology, 262(1), 187-193. doi:10.1007/s00415-014-7547-9.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0026-AACF-C Version Permalink: http://hdl.handle.net/11858/00-001M-0000-002A-5857-3
Genre: Journal Article

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Wilcox.pdf (Publisher version), 279KB
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© 2014 Springer International Publishing AG, Part of Springer Science+Business Media
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 Creators:
Wilcox, R., Author
Brænne, I., Author
Brüggemann, N., Author
Winkler, S., Author
Wiegers, K., Author
Bertram, L.1, Author              
Anderson, T., Author
Lohmann, K., Author
Affiliations:
1Neuropsychiatric Genetics (Lars Bertram), Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479655              

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Language(s): eng - English
 Dates: 2014-10-312015-01-01
 Publication Status: Published in print
 Pages: 6
 Publishing info: -
 Table of Contents: -
 Rev. Method: Peer
 Identifiers: DOI: 10.1007/s00415-014-7547-9
 Degree: -

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Title: Journal of Neurology
Source Genre: Journal
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Publ. Info: Berlin [etc.] : Springer
Pages: 6 Volume / Issue: 262 (1) Sequence Number: - Start / End Page: 187 - 193 Identifier: ISSN: 0340-5354
CoNE: https://pure.mpg.de/cone/journals/resource/110978979590419