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Novel presenilin 1 mutation with profound neurofibrillary pathology in an indigenous Southern African family with early-onset Alzheimer\u27s disease
Authors
de Villiers C
Heckmann JM
+7Â more
Kalaria RN
Low WC
Morris CM
Ramesar RS
Rao H
Rutherfoord S
Vorster A
Publication date
21 October 2003
Publisher
'Oxford University Press (OUP)'
Abstract
Abstract is not available.
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oai:eprints.ncl.ac.uk:86357
Last time updated on 30/05/2021