Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy. (Q36719106)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18514161%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

Hyperglycosylation and reduced GABA currents of mutated GABRB3 polypeptide in remitting childhood absence epilepsy (English)

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8 January 2020

3

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Reyna M Duron

6

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8 January 2020

Iris E Martínez-Juárez

8

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Aurelio Jara-Prado

15

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Antonio V Delgado-Escueta

8 January 2020

18

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8 January 2020

author name string

Miyabi Tanaka

1

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8 January 2020

Richard W Olsen

2

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8 January 2020

Emily Schwartz

4

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8 January 2020

Maria Elisa Alonso

5

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8 January 2020

Ramon Castro-Ortega

7

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8 January 2020

Ignacio Pascual-Castroviejo

9

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8 January 2020

Jesus Machado-Salas

10

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8 January 2020

Rene Silva

11

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8 January 2020

Julia N Bailey

12

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8 January 2020

Dongsheng Bai

13

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8 January 2020

Adriana Ochoa

14

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8 January 2020

Gregorio Pineda

16

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8 January 2020

Robert L Macdonald

17

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8 January 2020

language of work or name

English

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publication date

1 June 2008

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American Journal of Human Genetics

8 January 2020

published in

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volume

82

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8 January 2020

issue

6

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8 January 2020

page(s)

1249-1261

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describes a project that uses

8 January 2020

ImageQuant

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11 June 2022

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inferred from PubMed Central ID database lookup

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5 September 2018

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5 September 2018

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Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

5 September 2018

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5 September 2018

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A mutation in the GABA(A) receptor alpha(1)-subunit is associated with absence epilepsy

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Identifiers

DOI

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8 January 2020

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8 January 2020

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