18704120

Source:http://linkedlifedata.com/resource/pubmed/id/18704120

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0035334, umls-concept:C0205381, umls-concept:C0242960, umls-concept:C0443147
pubmed:issue	1
pubmed:dateCreated	2009-1-16
pubmed:abstractText	To define molecular and ophthalmic features of a rare phenotype in autosomal dominant (ad) retinitis pigmentosa (RP).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8703986
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1476-5454
pubmed:author	pubmed-author:AlemanT STS, pubmed-author:CideciyanA VAV, pubmed-author:JacobsonS GSG, pubmed-author:LamB LBL, pubmed-author:RomanA JAJ, pubmed-author:SchwartzS BSB, pubmed-author:StoneE MEM, pubmed-author:SumarokaAA, pubmed-author:WindsorE A MEA
pubmed:issnType	Electronic
pubmed:volume	23
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	230-3
pubmed:dateRevised	2009-11-3
pubmed:meshHeading	pubmed-meshheading:18704120-Adult, pubmed-meshheading:18704120-Chromosome Disorders, pubmed-meshheading:18704120-Electroretinography, pubmed-meshheading:18704120-Female, pubmed-meshheading:18704120-Heterozygote, pubmed-meshheading:18704120-Humans, pubmed-meshheading:18704120-Pedigree, pubmed-meshheading:18704120-Retinitis Pigmentosa
pubmed:year	2009
pubmed:articleTitle	Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic wavelets.
pubmed:affiliation	Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, PA 19104, USA. aleman@mail.med.upenn.edu
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't