Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2008-2-6
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0013-9580
pubmed:author
pubmed:issnType
Print
pubmed:volume
49
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
360-5
pubmed:dateRevised
2008-4-23
pubmed:meshHeading
pubmed-meshheading:18251839-Adult, pubmed-meshheading:18251839-Age of Onset, pubmed-meshheading:18251839-Aged, pubmed-meshheading:18251839-Child, pubmed-meshheading:18251839-Child, Preschool, pubmed-meshheading:18251839-Comorbidity, pubmed-meshheading:18251839-Death, Sudden, pubmed-meshheading:18251839-Death, Sudden, Cardiac, pubmed-meshheading:18251839-Epilepsy, Generalized, pubmed-meshheading:18251839-Female, pubmed-meshheading:18251839-Genetic Markers, pubmed-meshheading:18251839-Genetic Predisposition to Disease, pubmed-meshheading:18251839-Haplotypes, pubmed-meshheading:18251839-Humans, pubmed-meshheading:18251839-Male, pubmed-meshheading:18251839-Mutation, pubmed-meshheading:18251839-Nerve Tissue Proteins, pubmed-meshheading:18251839-Pedigree, pubmed-meshheading:18251839-Risk Factors, pubmed-meshheading:18251839-Seizures, Febrile, pubmed-meshheading:18251839-Sodium Channels
pubmed:year
2008
pubmed:articleTitle
Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation.
pubmed:publicationType
Letter, Comparative Study