10874321

Source:http://linkedlifedata.com/resource/pubmed/id/10874321

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0026882, umls-concept:C0035334, umls-concept:C0339530, umls-concept:C1413723, umls-concept:C1527180, umls-concept:C1711254
pubmed:issue	1
pubmed:dateCreated	2000-8-25
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/cone rod homeobox protein
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1098-1004
pubmed:author	pubmed-author:CormandBB, pubmed-author:HämäläinenR HRH, pubmed-author:IgnatiusJJ, pubmed-author:JoensuuT HTH, pubmed-author:RaitanenNN, pubmed-author:SankilaE MEM, pubmed-author:ValleOO
pubmed:issnType	Electronic
pubmed:volume	16
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	94
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:10874321-Adolescent, pubmed-meshheading:10874321-Age of Onset, pubmed-meshheading:10874321-Child, pubmed-meshheading:10874321-Child, Preschool, pubmed-meshheading:10874321-Finland, pubmed-meshheading:10874321-Genes, Dominant, pubmed-meshheading:10874321-Homeodomain Proteins, pubmed-meshheading:10874321-Humans, pubmed-meshheading:10874321-Mutation, pubmed-meshheading:10874321-Retinitis Pigmentosa, pubmed-meshheading:10874321-Trans-Activators
pubmed:year	2000
pubmed:articleTitle	A CRX mutation in a Finnish family with dominant cone-rod retinal dystrophy.
pubmed:affiliation	Department of Medical Genetics, University of Helsinki, Helsinki, Finland.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't