12244629

Source:http://linkedlifedata.com/resource/pubmed/id/12244629

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0743559, umls-concept:C1864923
pubmed:issue	15
pubmed:dateCreated	2002-9-24
pubmed:language	fin
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0373207
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CLN8 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Cln8 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
pubmed:status	MEDLINE
pubmed:issn	0012-7183
pubmed:author	pubmed-author:HaltiaMattiM, pubmed-author:HervaRiittaR, pubmed-author:HirvasniemiAuneA, pubmed-author:LehesjokiAnna-ElinaAE, pubmed-author:RantaSusannaS
pubmed:issnType	Print
pubmed:volume	118
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1551-8
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:12244629-Animals, pubmed-meshheading:12244629-Epilepsy, pubmed-meshheading:12244629-Finland, pubmed-meshheading:12244629-Humans, pubmed-meshheading:12244629-Intellectual Disability, pubmed-meshheading:12244629-Membrane Proteins, pubmed-meshheading:12244629-Mice, pubmed-meshheading:12244629-Neuronal Ceroid-Lipofuscinoses, pubmed-meshheading:12244629-Pedigree, pubmed-meshheading:12244629-Point Mutation, pubmed-meshheading:12244629-Prognosis, pubmed-meshheading:12244629-Syndrome
pubmed:year	2002
pubmed:articleTitle	[Northern epilepsy and the gene error behind it].
pubmed:affiliation	Folkhälsanin perinnöllisyystieteen laitos, Haartman-instituutti, lääketieteellisen genetiikan osasto Biomedicum Helsinki PL 63, 00014 Helsingin yliopisto sekä Jorvin sairaala 02740 Espoo. susanna.ranta@helsinki.fi
pubmed:publicationType	Journal Article, Review