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 ORCID: https://orcid.org/0000-0003-2062-8623, Morris, H. R., White, C., Smith, Philip E. M. ORCID: https://orcid.org/0000-0003-4250-2562 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:	01 Nov 2022 09:40
URI:	https://orca.cardiff.ac.uk/id/eprint/88811

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