Edinburgh Research Explorer

Anna Williams

Personal chair of Regenerative neurology

  1. 2001
  2. A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease

    Guilbot, A., Williams, A., Ravisé, N., Verny, C., Brice, A., Sherman, D. L., Brophy, P. J., LeGuern, E., Delague, V., Bareil, C., Mégarbané, A. & Claustres, M., 15 Feb 2001, In : Human Molecular Genetics. 10, 4, p. 415-21 7 p.

    Research output: Contribution to journalArticle

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