Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit α4 with common idiopathic generalized epilepsies (Q73592109)

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scientific article published on July 25, 1997

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English	Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit α4 with common idiopathic generalized epilepsies	scientific article published on July 25, 1997

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scholarly article

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5 November 2019

Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies (English)

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5 November 2019

Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit α4 with common idiopathic generalized epilepsies (English)

1 reference

10.1002/(SICI)1096-8628(19970725)74:4<445::AID-AJMG18>3.0.CO;2-I

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11 November 2024

restriction fragment length polymorphism

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11 November 2024

author name string

O. Steinlein

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11 November 2024

T. Sander

2

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11 November 2024

J. Stoodt

3

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11 November 2024

R. Kretz

4

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11 November 2024

D. Janz

5

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11 November 2024

P. Propping

6

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11 November 2024

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11 November 2024

publication date

1 July 1997

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5 November 2019

25 July 1997

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11 November 2024

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10.1002/(SICI)1096-8628(19970725)74:4<445::AID-AJMG18>3.0.CO;2-I

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11 November 2024

https://onlinelibrary.wiley.com/doi/full/10.1002/(SICI)1096-8628(19970725)74:4%3C445::AID-AJMG18%3E3.0.CO;2-I

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10.1002/(SICI)1096-8628(19970725)74:4<445::AID-AJMG18>3.0.CO;2-I

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11 November 2024

American Journal of Medical Genetics Part A

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5 November 2019

74

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5 November 2019

4

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5 November 2019

445-449

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

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Progress in mapping human epilepsy genes

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

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Idiopathic generalized epilepsy of adolescence: are the syndromes clinically distinct?

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Detection of a CfoI polymorphism within exon 5 of the human neuronal nicotinic acetylcholine receptor ?4 subunit gene (CHRNA4)

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

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Identifiers

10.1002/(SICI)1096-8628(19970725)74:4<445::AID-AJMG18>3.0.CO;2-I

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9259383%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9259383%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

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