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The R110C mutation in Notch3 causes variable clinical features in two Turkish families with CADASIL syndrome.

Authors
Type
Published Article
Journal
Journal of the Neurological Sciences
0022-510X
Publisher
Elsevier
Publication Date
Volume
246
Issue
1-2
Pages
123–130
Identifiers
PMID: 16730748
Source
Medline

Abstract

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