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Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL

Journal article
Authors W.C. Low
M. Junna
Anne Börjesson-Hanson
C.M. Morris
T.H. Moss
D.L. Stevens
D. St. Clair
T. Mizuno
W.W. Zhang
K. Mykkänen
Jan Wahlström
Oluf Andersen
Hannu Kalimo
M. Viitanen
R.N. Kalaria
Published in BRAIN
Volume 130
Pages 357-367
ISSN 0006-8950
Publication year 2007
Published at Institute of Biomedicine, Department of Medical and Clinical Genetics
Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Pages 357-367
Language en
Links dx.doi.org/10.1093/brain/awl360
Keywords autosomal-dominant arteriopathy, small-vessel disease, subcortical infarcts, cerebroretinal vasculopathy, vascular retinopathy, alzheimers-disease, leukoencephalopathy, mutations, stroke, pathology
Subject categories Neurology, Neuroscience
Page Manager: Webmaster|Last update: 9/11/2012
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