| Property |
Value |
| dbo:abstract
|
- le gène humain SCN1A, code la protéine du canal sodium, voltage-dépendant, type I, sous-unité alpha. (fr)
- le gène humain SCN1A, code la protéine du canal sodium, voltage-dépendant, type I, sous-unité alpha. (fr)
|
| dbo:wikiPageExternalLink
| |
| dbo:wikiPageID
| |
| dbo:wikiPageLength
|
- 17510 (xsd:nonNegativeInteger)
|
| dbo:wikiPageRevisionID
| |
| dbo:wikiPageWikiLink
| |
| prop-fr:année
|
- 1994 (xsd:integer)
- 2001 (xsd:integer)
- 2004 (xsd:integer)
|
| prop-fr:bibcode
| |
| prop-fr:date
|
- December 2001 (fr)
- May 1992 (fr)
- June 2001 (fr)
- June 2005 (fr)
- April 2001 (fr)
- August 2001 (fr)
- October 1999 (fr)
- October 1986 (fr)
- July 2004 (fr)
- December 2005 (fr)
- March 2001 (fr)
- January 2002 (fr)
- December 2001 (fr)
- May 1992 (fr)
- June 2001 (fr)
- June 2005 (fr)
- April 2001 (fr)
- August 2001 (fr)
- October 1999 (fr)
- October 1986 (fr)
- July 2004 (fr)
- December 2005 (fr)
- March 2001 (fr)
- January 2002 (fr)
|
| prop-fr:doi
|
- 10.100200 (xsd:double)
- 10.101600 (xsd:double)
- 10.107300 (xsd:double)
- 10.108600 (xsd:double)
- 10.112400 (xsd:double)
- 10.115900 (xsd:double)
- 10.121200 (xsd:double)
- 10.274100 (xsd:double)
|
| prop-fr:lireEnLigne
| |
| prop-fr:numéro
|
- 1 (xsd:integer)
- 2 (xsd:integer)
- 3 (xsd:integer)
- 4 (xsd:integer)
- 6 (xsd:integer)
- 12 (xsd:integer)
- 19 (xsd:integer)
|
| prop-fr:pages
|
- 12 (xsd:integer)
- 15 (xsd:integer)
- 37 (xsd:integer)
- 53 (xsd:integer)
- 103 (xsd:integer)
- 146 (xsd:integer)
- 178 (xsd:integer)
- 329 (xsd:integer)
- 397 (xsd:integer)
- 535 (xsd:integer)
- 671 (xsd:integer)
- 703 (xsd:integer)
- 859 (xsd:integer)
- 866 (xsd:integer)
- 1327 (xsd:integer)
- 2265 (xsd:integer)
- 7503 (xsd:integer)
|
| prop-fr:pmcid
|
- 386747 (xsd:integer)
- 1226119 (xsd:integer)
- 1275639 (xsd:integer)
- 1275640 (xsd:integer)
|
| prop-fr:pmid
|
- 1317301 (xsd:integer)
- 2429308 (xsd:integer)
- 8062593 (xsd:integer)
- 10514109 (xsd:integer)
- 11254444 (xsd:integer)
- 11254445 (xsd:integer)
- 11295230 (xsd:integer)
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- 11823106 (xsd:integer)
- 15277629 (xsd:integer)
- 15508916 (xsd:integer)
- 15880351 (xsd:integer)
- 16382098 (xsd:integer)
|
| prop-fr:périodique
|
- FEBS Letters (fr)
- Proceedings of the National Academy of Sciences of the United States of America (fr)
- Human Mutation (fr)
- American Journal of Medical Genetics (fr)
- Neurology (fr)
- American Journal of Human Genetics (fr)
- Pharmacological Reviews (fr)
- Advances in Neurology (fr)
- Annals of Neurology (fr)
- Brain Research. Molecular Brain Research (fr)
- Cytogenetics and Cell Genetics (fr)
- Epilepsy Research (fr)
- Frontiers in Bioscience (fr)
- FEBS Letters (fr)
- Proceedings of the National Academy of Sciences of the United States of America (fr)
- Human Mutation (fr)
- American Journal of Medical Genetics (fr)
- Neurology (fr)
- American Journal of Human Genetics (fr)
- Pharmacological Reviews (fr)
- Advances in Neurology (fr)
- Annals of Neurology (fr)
- Brain Research. Molecular Brain Research (fr)
- Cytogenetics and Cell Genetics (fr)
- Epilepsy Research (fr)
- Frontiers in Bioscience (fr)
|
| prop-fr:titre
|
- Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus (fr)
- Localization of a putative human brain sodium channel gene to chromosome band 2q24 (fr)
- Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation (fr)
- Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort (fr)
- Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures (fr)
- Ion channels and epilepsy (fr)
- SCN1A mutations and epilepsy (fr)
- The role of sodium channels in cell adhesion (fr)
- Differential expression of two sodium channel subtypes in human brain (fr)
- International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels (fr)
- A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy (fr)
- Comparative distribution of voltage-gated sodium channel proteins in human brain (fr)
- De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy (fr)
- Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity (fr)
- A locus for febrile seizures maps to chromosome 2q23-24 (fr)
- Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes (fr)
- Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the -channel alpha 1 subunit gene, SCN1A (fr)
- Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus (fr)
- Localization of a putative human brain sodium channel gene to chromosome band 2q24 (fr)
- Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation (fr)
- Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort (fr)
- Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures (fr)
- Ion channels and epilepsy (fr)
- SCN1A mutations and epilepsy (fr)
- The role of sodium channels in cell adhesion (fr)
- Differential expression of two sodium channel subtypes in human brain (fr)
- International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels (fr)
- A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy (fr)
- Comparative distribution of voltage-gated sodium channel proteins in human brain (fr)
- De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy (fr)
- Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity (fr)
- A locus for febrile seizures maps to chromosome 2q23-24 (fr)
- Messenger RNA coding for only the alpha subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes (fr)
- Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the -channel alpha 1 subunit gene, SCN1A (fr)
|
| prop-fr:volume
|
- 7 (xsd:integer)
- 25 (xsd:integer)
- 46 (xsd:integer)
- 48 (xsd:integer)
- 57 (xsd:integer)
- 63 (xsd:integer)
- 67 (xsd:integer)
- 68 (xsd:integer)
- 83 (xsd:integer)
- 88 (xsd:integer)
- 95 (xsd:integer)
- 106 (xsd:integer)
- 303 (xsd:integer)
|
| prop-fr:wikiPageUsesTemplate
| |
| dct:subject
| |
| rdf:type
| |
| rdfs:comment
|
- le gène humain SCN1A, code la protéine du canal sodium, voltage-dépendant, type I, sous-unité alpha. (fr)
- le gène humain SCN1A, code la protéine du canal sodium, voltage-dépendant, type I, sous-unité alpha. (fr)
|
| rdfs:label
| |
| rdfs:seeAlso
| |
| owl:sameAs
| |
| prov:wasDerivedFrom
| |
| foaf:isPrimaryTopicOf
| |
| is dbo:wikiPageRedirects
of | |
| is dbo:wikiPageWikiLink
of | |
| is oa:hasTarget
of | |
| is foaf:primaryTopic
of | |
