Behnam M, Ghorbani F, Shin JH, Kim DS, Jang H, Nouri N, Sedghi M, Salehi M, Ansari B, Basiri K. Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation. Gene. 2015 Oct 1;570(1):150-2. Epub 2015 Jun 15 PubMed.

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Mutations

  1. MAPT R406W