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Neurology. Genetics, 2376-7839


  1. De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity

    Ladds, E., Whitney, A., Dombi, E., Hofer, M., Anand, G., Harrison, V., Fratter, C., Carver, J., Barbosa, I. A., Simpson, M., Jayawant, S. & Poulton, J., 1 Aug 2018, In : Neurology: Genetics. 4, 4, e258.

    Research output: Contribution to journalArticle

  2. Genetics of stroke in a UK African ancestry case-control study: South London Ethnicity and Stroke Study

    Traylor, M., Rutten-Jacobs, L., Curtis, C., Patel, H., Breen, G., Newhouse, S., Lewis, C. M. & Markus, H. S., Apr 2017, In : Neurol Genet. 3, 2, p. e142

    Research output: Contribution to journalArticle

  3. Analysis of rare copy number variation in absence epilepsies

    Addis, L., Rosch, R. E., Valentin, A., Makoff, A., Robinson, R., Everett, K. V., Nashef, L. & Pal, D. K., Apr 2016, In : Neurology. Genetics. 2, 2, e56.

    Research output: Contribution to journalArticle

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