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    Young, T., Shuey, N., Partridge, J., Bremner, F. D., & Nicholl, D. J. (2013). compound Charcot-Marie-Tooth disease: a kindred with severe hereditary neuropathy, pupil abnormalities and a novel MPZ mutation. Journal of neurology, neurosurgery and psychiatry, 84(2), 234–236. http://access.bl.uk/ark:/81055/vdc_100137788700.0x00003c
  
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