KCNT1 mutations in ADNFLE and MMPSI: a new driver in the etiology and pathophysiology of early-onset epileptic syndromes. (Q45022179)

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English	KCNT1 mutations in ADNFLE and MMPSI: a new driver in the etiology and pathophysiology of early-onset epileptic syndromes.	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

23278465

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

title

KCNT1 mutations in ADNFLE and MMPSI: a new driver in the etiology and pathophysiology of early-onset epileptic syndromes (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23278465

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

main subject

pathophysiology

1 reference

based on heuristic

inferred from title

Malignant Migrating Partial Seizures in Infancy

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based on heuristic

inferred from title

author

Folefac Aminkeng

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23278465

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

author name string

F Aminkeng

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23278465

retrieved

8 December 2017

publication date

24 January 2013

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23278465

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

published in

Clinical Genetics

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stated in

Europe PubMed Central

PubMed publication ID

23278465

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

volume

83

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stated in

Europe PubMed Central

PubMed publication ID

23278465

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

issue

4

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stated in

Europe PubMed Central

PubMed publication ID

23278465

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

page(s)

319-320

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Europe PubMed Central

PubMed publication ID

23278465

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

cites work

Channelopathies in idiopathic epilepsy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FCGE.12082

retrieved

21 January 2018

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FCGE.12082

retrieved

21 January 2018

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FCGE.12082

retrieved

21 January 2018

Identifiers

DOI

10.1111/CGE.12082

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23278465

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

PubMed publication ID

23278465

1 reference

stated in

Europe PubMed Central

PubMed publication ID

23278465

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23278465%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 February 2020

ResearchGate publication ID

234030089

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