(Q56770106)

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Notch3 mutations and the potential for diagnostic testing for CADASIL

scientific article published in The Lancet

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Europe PubMed Central

PubMed publication ID

9388391

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

title

Notch3 mutations and the potential for diagnostic testing for CADASIL (English)

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stated in

Europe PubMed Central

PubMed publication ID

9388391

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

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7 November 2019

main subject

diagnosis

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English

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publication date

1 November 1997

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Europe PubMed Central

PubMed publication ID

9388391

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

Europe PubMed Central

PubMed publication ID

9388391

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

volume

350

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Europe PubMed Central

PubMed publication ID

9388391

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

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7 November 2019

issue

9090

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Europe PubMed Central

PubMed publication ID

9388391

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

page(s)

1490

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Europe PubMed Central

PubMed publication ID

9388391

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

cites work

Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2922047-7

retrieved

7 January 2021

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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

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Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2922047-7

retrieved

7 January 2021

based on heuristic

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Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2922047-7

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2897%2922047-7

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0140-6736(97)22047-7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9388391

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 November 2019

PubMed publication ID

9388391

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9388391

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9388391%20AND%20SRC:MED&resulttype=core&format=json

(Q56770106)

Notch3 mutations and the potential for diagnostic testing for CADASIL

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