A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementia

Annals of the New York Academy of Sciences

Volumn 903, Issue , 2000, Pages 129-137

  Ghiso, J ^a   Vidal, R ^a   Rostagno, A ^a   Mead, S ^b   Revesz T ^c   Plant, G ^c   Frangione, B ^a  

^a NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; AMYLOID PRECURSOR PROTEIN; AMYLOID PROTEIN; PROTEIN SUBUNIT;

CEREBELLAR ATAXIA; CHROMOSOME 13; COGNITIVE DEFECT; CONFERENCE PAPER; DEMENTIA; FAMILIAL DISEASE; GENE MUTATION; HIPPOCAMPUS; HUMAN; NUCLEIC ACID BASE SUBSTITUTION; OPEN READING FRAME; SPASTICITY; STOP CODON;

ATAXIA;

EID: 0034060296     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2000.tb06359.x     Document Type: Conference Paper

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