(Q39863856)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

title

New mutation of the Na channel in the severe form of potassium-aggravated myotonia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

author name string

Masanobu Kinoshita

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

Ryogen Sasaki

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

Futoshi Aoike

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

Masanori P Takahashi

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

Saburo Sakoda

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

Kazuhiko Hirose

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

language of work or name

1 reference

1 May 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

volume

39

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

page(s)

666-673

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19347921%20AND%20SRC:MED&resulttype=core&format=json

Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndrome

25 January 2020

cites work

1 reference

Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5

21 January 2018

1 reference

Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker

21 January 2018

1 reference

K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation

21 January 2018

1 reference

Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channel

21 January 2018

1 reference

21 January 2018

1 reference

Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy

21 January 2018

1 reference

Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.

21 January 2018

1 reference