High frequency of mutations in four different disease genes in early-onset dementia

Annals of the New York Academy of Sciences

Volumn 920, Issue , 2000, Pages 100-106

  Finckh, Ulrich ^a   Müller Thomsen, Tomas ^a   Mann, Ulrike ^a   Eggers, Christian ^b   Marksteiner, Josef ^c   Meins, Wolfgang ^d   Binetti, Giuliano ^e   Alberici, Antonella ^e   Sonderegger, Peter ^a   Hock, Christoph ^a   Nitsch, Roger M ^a   Andreas, G A L ^b  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b UNIVERSITY OF INNSBRUCK   (Austria)

^c ALBERTINEN KRANKENHAUS   (Germany)

^d IRCCS ISTITUTO CENTRO SAN GIOVANNI DI DIO FATEBENEFRATELLI   (Italy)

^e UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID PRECURSOR PROTEIN; GENE PRODUCT; NEUROSERPIN; PRESENILIN 1; PRESENILIN 2; PRION PROTEIN; TAU PROTEIN; UNCLASSIFIED DRUG;

AUTOPSY; CLINICAL ARTICLE; CONFERENCE PAPER; CONTROLLED STUDY; DEATH; DEMENTIA; DISEASE MARKER; FAMILY HISTORY; GENE FREQUENCY; GENE MUTATION; GENETIC SCREENING; HETEROZYGOSITY; HISTOPATHOLOGY; HUMAN; HUMAN CELL; ONSET AGE; PREDICTION; PRION DISEASE; PROTEIN ANALYSIS;

EID: 0034534680     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2000.tb06910.x     Document Type: Conference Paper

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