Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

Ítems similars

• Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filaments
  per: Spillantini, Maria Grazia, et al.
  Publicat: (1997)
• Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.
  per: Murrell, J R, et al.
  Publicat: (1997)
• The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family
  per: Spina, Salvatore, et al.
  Publicat: (2008)
• Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17
  per: Varani, Luca, et al.
  Publicat: (1999)
• Analysis of Tau Phosphorylation and Truncation in a Mouse Model of Human Tauopathy
  per: Delobel, Patrice, et al.
  Publicat: (2008)