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PATH42 Lineage, clinical, genetic, structural and cellular characterisation of a novel epilepsy mutation [Conference Abstract]

Johnston, J. A., Davies, J. S., Baer, K., Hammond, C. L., Mullins, J. G. L., Cushion, T. D., Chung, S. K., Thomas, Rhys Huw, Morris, H. R., White, C., Smith, Philip E. M. and Rees, M. I. 2010. PATH42 Lineage, clinical, genetic, structural and cellular characterisation of a novel epilepsy mutation [Conference Abstract]. Journal of Neurology, Neurosurgery & Psychiatry 81 (11) , e19-e19.

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Item Type: Article
Date Type: Publication
Status: Published
Schools: MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Medicine
Subjects: R Medicine > R Medicine (General)
R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
Publisher: BMJ Publishing Group
ISSN: 0022-3050
Last Modified: 04 Jun 2017 08:59
URI: http://orca.cf.ac.uk/id/eprint/88811

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