Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: A comparison of the pallidopontonigral degeneration kindred and a French family

Archives of Neurology

Volumn 59, Issue 6, 2002, Pages 943-950

  Tsuboi, Yoshio ^a   Uitti, Ryan J ^a   Delisle, Marie Bernadette ^b   Ferreira, Joaquim J ^c   Brefel Courbon, Christine ^c   Rascol, Olivier ^c   Ghetti, Bernardino ^d   Murrell, Jill R ^d   Hutton, Michael ^a   Baker, Matthew ^a   Wszolek, Zbigniew K ^a  

^a MAYO CLINIC   (United States)

^b CHU RANGUEIL   (France)

^c CHU PURPAN   (France)

^d INDIANA UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TAU PROTEIN;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CHROMOSOME 17; CLINICAL FEATURE; DEGENERATIVE DISEASE; EXON; FAMILY; FRANCE; GENE MUTATION; GENEALOGY; GENETIC LINKAGE; HAPLOTYPE; HUMAN; MALE; MICROSATELLITE MARKER; MISSENSE MUTATION; MOLECULAR GENETICS; ONSET AGE; PALLIDOPONTONIGRAL DEGENERATION; PRIORITY JOURNAL;

EID: 0036279601     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.59.6.943     Document Type: Article

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