Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24. (Q48098135)

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31 October 2019

title

Exclusion of the JRK/JH8 gene as a candidate for human childhood absence epilepsy mapped on 8q24 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10510981%20AND%20SRC:MED&resulttype=core&format=json

childhood absence epilepsy

31 October 2019

main subject

1 reference

Antonio V Delgado-Escueta

inferred from title

author

5

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31 October 2019

Kazuhiro Yamakawa

6

1 reference

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31 October 2019

author name string

R Morita

1

1 reference

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31 October 2019

E Miyazaki

2

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31 October 2019

P U Shah

3

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31 October 2019

I P Castroviejo

4

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31 October 2019

publication date

1 November 1999

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31 October 2019

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31 October 2019

volume

37

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31 October 2019

issue

2

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31 October 2019

page(s)

151-158

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

31 October 2019

cites work

1 reference

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7 January 2021

Sensitivity to jerky gene dosage underlies epileptic seizures in mice

1 reference

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7 January 2021

Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.

1 reference

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7 January 2021

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

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7 January 2021

Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations

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7 January 2021

Genetics of convulsive disorders. II. Genetic and electroencephalographic studies in centrencephalic epilepsy

1 reference

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7 January 2021

JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900061-3

7 January 2021

Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice

1 reference

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7 January 2021

A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history

1 reference

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7 January 2021

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21

1 reference

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7 January 2021

Mapping of genes predisposing to idiopathic generalized epilepsy

1 reference

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7 January 2021

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Identifiers

DOI

1 reference

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31 October 2019

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