De novo mutation in theNotch3 gene causing CADASIL (Q29303133)

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scientific article (publication date: March 2000)

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Language	Label	Description	Also known as
English	De novo mutation in theNotch3 gene causing CADASIL	scientific article (publication date: March 2000)

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De novo mutation in theNotch3 gene causing CADASIL (English)

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https://doi.org/10.1002%2F1531-8249%28200003%2947%3A3%3C388%3A%3AAID-ANA19%3E3.0.CO%3B2-Q

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9 April 2017

author

Marie-Germaine Bousser

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6

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Elisabeth Tournier-Lasserve

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5

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Elisabeth Tournier-Lasserve

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9 April 2017

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https://doi.org/10.1002%2F1531-8249%28200003%2947%3A3%3C388%3A%3AAID-ANA19%3E3.0.CO%3B2-Q

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Anne Joutel

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1

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https://doi.org/10.1002%2F1531-8249%28200003%2947%3A3%3C388%3A%3AAID-ANA19%3E3.0.CO%3B2-Q

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9 April 2017

David D. Dodick

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2

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https://doi.org/10.1002%2F1531-8249%28200003%2947%3A3%3C388%3A%3AAID-ANA19%3E3.0.CO%3B2-Q

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9 April 2017

Joseph E. Parisi

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3

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9 April 2017

Michaelle Cecillon

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4

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9 April 2017

publication date

March 2000

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9 April 2017

published in

Annals of Neurology

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9 April 2017

volume

47

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issue

3

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9 April 2017

page(s)

388-391

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9 April 2017

cites work

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy

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Crossref

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https://api.crossref.org/works/10.1002%2F1531-8249%28200003%2947%3A3%3C388%3A%3AAID-ANA19%3E3.0.CO%3B2-Q

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21 January 2018

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study

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https://api.crossref.org/works/10.1002%2F1531-8249%28200003%2947%3A3%3C388%3A%3AAID-ANA19%3E3.0.CO%3B2-Q

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21 January 2018

Identifiers

DOI

10.1002/1531-8249(200003)47:3<388::AID-ANA19>3.0.CO;2-Q

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https://doi.org/10.1002%2F1531-8249%28200003%2947%3A3%3C388%3A%3AAID-ANA19%3E3.0.CO%3B2-Q

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9 April 2017

 

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