(Q28295745)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647781%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2. (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647781%20AND%20SRC:MED&resulttype=core&format=json

autosomal dominant nocturnal frontal lobe epilepsy

22 October 2019

main subject

0 references

author

Ingrid Scheffer

2

1 reference

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22 October 2019

author name string

Phillips HA

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647781%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Berkovic SF

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647781%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Hollway GE

4

1 reference

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22 October 2019

Sutherland GR

5

1 reference

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22 October 2019

Mulley JC

6

1 reference

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22 October 2019

language of work or name

English

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publication date

1 May 1995

1 reference

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22 October 2019

1 reference

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22 October 2019

volume

10

1 reference

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22 October 2019

page(s)

117-118

1 reference

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22 October 2019

issue

1

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng0595-117

22 October 2019

exact match

0 references

cites work

Refinement of the localization of the gene for neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) to human chromosome 20q13.2-q13.3

1 reference

https://api.crossref.org/works/10.1038/NG0595-117

Localization of the genes encoding the melanocortin-2 (adrenocorticotropic hormone) and melanocortin-3 receptors to chromosomes 18p11.2 and 20q13.2-q13.3 by fluorescence in situ hybridization

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0595-117

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Genes for epilepsy mapped in the mouse.

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Phenotypic diversity, allelic series and modifier genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Localization of a gene for the human low-voltage EEG on 20q and genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

A nonsense mutation in the alpha4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Chromosomal localization of seven neuronal nicotinic acetylcholine receptor subunit genes in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Chromosomal localization of mouse and human neurotensin receptor genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1038%2FNG0595-117

7 January 2021

Identifiers

DOI

10.1038/NG0595-117

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647781%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference