(Q28212831)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

Sodium channels SCN1A, SCN2A and SCN3A in familial autism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

0 references

8

1 reference

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31 October 2019

author name string

Weiss LA

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Escayg A

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Kearney JA

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Trudeau M

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

MacDonald BT

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Mori M

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Reichert J

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Meisler MH

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

language of work or name

English

0 references

publication date

1 February 2003

1 reference

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31 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

page(s)

186-194

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12610651%20AND%20SRC:MED&resulttype=core&format=json

Autism spectrum disorders

31 October 2019

cites work

1 reference

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Magnetoencephalographic patterns of epileptiform activity in children with regressive autism spectrum disorders

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Autism as a strongly genetic disorder: evidence from a British twin study

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21 January 2018

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Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

21 January 2018

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No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

21 January 2018

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Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

21 January 2018

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Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

21 January 2018

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A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

21 January 2018

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Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

21 January 2018

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A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy

21 January 2018

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Sodium channel alpha-subunit mRNAs I, II, III, NaG, Na6 and hNE (PN1): different expression patterns in developing rat nervous system.

21 January 2018

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Evolution and diversity of mammalian sodium channel genes

21 January 2018

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Identification of epilepsy genes in human and mouse

21 January 2018

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De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

21 January 2018

1 reference

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A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities.

21 January 2018

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The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

21 January 2018

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Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

21 January 2018

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Calcium channel beta 4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic

21 January 2018

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Characterization of human RNA splice signals by iterative functional selection of splice sites

21 January 2018

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Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia

21 January 2018

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Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

21 January 2018

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Altered subthreshold sodium currents and disrupted firing patterns in Purkinje neurons of Scn8a mutant mice

21 January 2018

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Sodium channels and neurological disease: insights from Scn8a mutations in the mouse

21 January 2018

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Are rare variants responsible for susceptibility to complex diseases?

21 January 2018

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21 January 2018

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7 January 2021

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

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7 January 2021

Distribution of voltage-gated sodium channel ?-subunit and ?-subunit mRNAs in human hippocampal formation, cortex, and cerebellum

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7 January 2021

Novel interaction of the voltage-dependent sodium channel (VDSC) with calmodulin: does VDSC acquire calmodulin-mediated Ca2+-sensitivity?

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7 January 2021

Functional effects of two voltage-gated sodium channel mutations that cause generalized epilepsy with febrile seizures plus type 2

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7 January 2021