(Q81892359)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18755274%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

title

A CACNB4 mutation shows that altered Ca(v)2.1 function may be a genetic modifier of severe myoclonic epilepsy in infancy (English)

1 reference

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13 January 2020

1 reference

1 reference

Iori Ohmori

1

1 reference

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13 January 2020

Mamoru Ouchida

2

1 reference

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13 January 2020

Takafumi Miki

3

1 reference

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13 January 2020

Nobuyoshi Mimaki

4

1 reference

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13 January 2020

Shigeki Kiyonaka

5

1 reference

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13 January 2020

Teiichi Nishiki

6

1 reference

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13 January 2020

Kazuhito Tomizawa

7

1 reference

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13 January 2020

Yasuo Mori

8

1 reference

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13 January 2020

Hideki Matsui

9

1 reference

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13 January 2020

publication date

3 August 2008

1 reference

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13 January 2020

published in

Neurobiology of Disease

1 reference

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13 January 2020

volume

32

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13 January 2020

issue

3

1 reference

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13 January 2020

page(s)

349-354

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18755274%20AND%20SRC:MED&resulttype=core&format=json

10.1016/J.NBD.2008.07.017

13 January 2020

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18755274%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

1 reference