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

Ghetti, B; Murrell, J R; Zolo, P; Spillantini, M G; Goedert, M

Ghetti, B; Murrell, J R; Zolo, P; Spillantini, M G; Goedert, M.

Affiliation

Ghetti B; Department of Pathology and Laboratory Medicine, Division of Neuropathology, Indiana University School of Medicine, 635 Barnhill Drive, MS A142, Indianapolis, IN 46202, USA. bghetti@iupui.edu

Ann N Y Acad Sci ; 920: 52-62, 2000.

Article in En | MEDLINE | ID: mdl-11193177

Subject(s)

Dementia/genetics; Mutation, Missense; Pick Disease of the Brain/genetics; tau Proteins/genetics; Adult; Amino Acid Substitution; Atrophy; Brain/pathology; Brain/ultrastructure; Dementia/pathology; Dementia/psychology; Frontal Lobe/pathology; Humans; Italy; Phenotype; Pick Disease of the Brain/pathology; Pick Disease of the Brain/psychology; Syndrome; Temporal Lobe/pathology

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Collection: 01-internacional Database: MEDLINE Main subject: Tau Proteins / Mutation, Missense / Pick Disease of the Brain / Dementia Type of study: Etiology_studies Limits: Adult / Humans Country/Region as subject: Europa Language: En Journal: Ann N Y Acad Sci Year: 2000 Type: Article Affiliation country: United States

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