Missense and splice site mutations in tau associated with FTDP-17: Multiple pathogenic mechanisms

Neurology

Volumn 56, Issue 11 SUPPL. 4, 2001, Pages

  Hutton, M ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TAU PROTEIN;

ARTICLE; CHROMOSOME 17; CLINICAL FEATURE; DELETION MUTANT; EXON; FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENETIC ANALYSIS; GENETIC PREDISPOSITION; HUMAN; MICROTUBULE; MISSENSE MUTATION; NERVE DEGENERATION; NEUROPATHOLOGY; PARKINSONISM; PRIORITY JOURNAL;

EID: 0034971707     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.56.suppl_4.s21     Document Type: Article

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