NDLI: Notch3 Mutations in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), a Mendelian Condition Causing Stroke and Vascular Dementia

Content Provider	Scilit
Author	Joutel, Anne Corpechot, Christophe Ducros, Anne Vahedi, Katayoun Chabriat, Hugues Mouton, Philippe Alamowitch, Sonia Domenga, Valérie Cécillion, Michaelle Maréchal, Emmanuelle Maciazek, Jacqueline Vayssière, Céline Cruaud, Corinne Cabanis, Emmanuel-Alain Ruchoux, Marie Madeleine Weissenbach, Jean Bach, Jean François Bousser, Marie Germaine Tournier-Lasserve, Elisabeth
Copyright Year	1997
Description	Journal: Annals of the New York Academy of Sciences
Related Links	https://nyaspubs.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1749-6632.1997.tb48472.x
Ending Page	217
Page Count	5
Starting Page	213
e-ISSN	17496632
DOI	10.1111/j.1749-6632.1997.tb48472.x
Journal	Annals of the New York Academy of Sciences
Issue Number	1
Volume Number	826
Language	English
Publisher	Wiley-Blackwell
Publisher Date	1997-09-01
Access Restriction	Open
Subject Keyword	Journal: Annals of the New York Academy of Sciences Clinical Neurology Cerebral Infarcts Vascular Dementia Leukoencephalopathy
Content Type	Text
Resource Type	Article

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Notch3 Mutations in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), a Mendelian Condition Causing Stroke and Vascular Dementia