Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chin...
Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese
About this item
Full title
Author / Creator
Lee, Y.-C. , Liu, C.-S. , Chang, M.-H. , Lin, K.-P. , Fuh, J.-L. , Lu, Y.-C. , Liu, Y.-F. and Soong, B.-W.
Publisher
Darmstadt: Steinkopff-Verlag
Journal title
Language
English
Formats
Publication information
Publisher
Darmstadt: Steinkopff-Verlag
Subjects
More information
Scope and Contents
Contents
Background and purpose
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary disorder caused by
NOTCH3
mutations and characterized by recurrent subcortical infarctions, dementia and leukoencephalopathy. So far, most clinical, molecular and neuroimaging information has come from...
Alternative Titles
Full title
Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_67032098
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_67032098
Other Identifiers
ISSN
0340-5354
E-ISSN
1432-1459
DOI
10.1007/s00415-009-0091-3
