Source:http://linkedlifedata.com/resource/pubmed/id/10904967
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2000-8-25
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pubmed:abstractText |
One of the recent findings in the investigation of epileptogenesis is the localization of new gene situses and mutations of the ion channels. The pathology of these ion channel disorders is responsible for a considerable number of disorders affecting the central nervous and musculoskeletal systems. Their clinical expression is often paroxystic. Mutations cause inactivation of the channel, which depending of the degree, conditions the phenotype of the disorder.
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pubmed:language |
spa
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0210-0010
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
30 Suppl 1
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
S42-6
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pubmed:dateRevised |
2009-5-28
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pubmed:meshHeading | |
pubmed:year |
2000
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pubmed:articleTitle |
[Clinical aspects of epileptic ion channel disorders].
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pubmed:affiliation |
Servicio de Neuropediatría, Hospital Clínico Universitario San Carlos, Madrid, España. jcampos@hcsc.insalud.es
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pubmed:publicationType |
Journal Article,
English Abstract,
Review
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