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Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variability

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References

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Authors and Affiliations

  1. Dept. of Neurology and Neuromuscular Diseases, Hôpital Universitaire Timone, Marseille, France

    W. Casseron,  J. P. Azulay & J. Pouget

  2. Dept. of Nuclear Medicine, Hôpital Universitaire Timone, Marseille, France

    E. Guedj

  3. Dept. of Neurology, Hôpital Universitaire Ste Marguerite, Marseille, France

    J. L. Gastaut

Authors
  1. W. Casseron
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  2. J. P. Azulay
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  3. E. Guedj
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  4. J. L. Gastaut
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  5. J. Pouget
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Corresponding author

Correspondence to J. P. Azulay.

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Casseron, W., Azulay, J.P., Guedj, E. et al. Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variability. J Neurol 252, 1546–1548 (2005). https://doi.org/10.1007/s00415-005-0880-2

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  • DOI: https://doi.org/10.1007/s00415-005-0880-2

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