Progress in hereditary tauopathies: A mutation in the Tau gene (G389R) causes a pick disease-like syndrome

Annals of the New York Academy of Sciences

Volumn 920, Issue , 2000, Pages 52-62

  Ghetti, Bernardino ^a,d   Murrell, Jill R ^b   Zolo, Paolo ^c   Spillantini, Maria Grazia ^a   Goedert, Michel ^b  

^a INDIANA UNIVERSITY   (United States)

^b ItalycUniversity of Cambridge   (United Kingdom)

^c MEDICAL RESEARCH COUNCIL   (United Kingdom)

^d INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; RECOMBINANT PROTEIN; TAU PROTEIN;

AMNESIA; APATHY; APHASIA; CLINICAL FEATURE; CONFERENCE PAPER; DEMENTIA; DEPHOSPHORYLATION; EXON; GENE MUTATION; GENETIC DISORDER; HEREDITARY TAUOPATHY; HUMAN; HUMAN CELL; HYPERPHAGIA; IMMUNOBLOTTING; IMMUNOREACTIVITY; MICROTUBULE; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PHENOTYPE; PICK PRESENILE DEMENTIA; PYRAMIDAL TRACT;

EID: 0034534951     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2000.tb06905.x     Document Type: Conference Paper

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