Edinburgh Research Explorer

James Withers

(Former employee or visitor)

  1. 2010
  2. Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis

    Chen, H-J., Anagnostou, G., Chai, A., Withers, J., Morris, A., Adhikaree, J., Pennetta, G. & de Belleroche, J. S., 17 Dec 2010, In : Journal of Biological Chemistry. 285, 51, p. 40266-40281 16 p.

    Research output: Contribution to journalArticle

  3. 2008
  4. hVAPB, the causative gene of a heterogeneous group of motor neuron diseases in humans, is functionally interchangeable with its Drosophila homologue DVAP-33A at the neuromuscular junction

    Chai, A., Withers, J., Koh, Y. H., Parry, K., Bao, H., Zhang, B., Budnik, V. & Pennetta, G., 15 Jan 2008, In : Human Molecular Genetics. 17, 2, p. 266-280 15 p.

    Research output: Contribution to journalArticle