Source:http://linkedlifedata.com/resource/pubmed/id/17932953
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2008-1-2
|
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
1531-8249
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
62
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
549-50
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:17932953-Calcium Channels, T-Type,
pubmed-meshheading:17932953-Channelopathies,
pubmed-meshheading:17932953-Epilepsy,
pubmed-meshheading:17932953-Genetic Testing,
pubmed-meshheading:17932953-Genetic Variation,
pubmed-meshheading:17932953-Humans,
pubmed-meshheading:17932953-Mutation, Missense,
pubmed-meshheading:17932953-Neurology
|
pubmed:year |
2007
|
pubmed:articleTitle |
Epilepsy genetics: yet more exciting news.
|
pubmed:publicationType |
Editorial,
Comment
|