11879142

Source:http://linkedlifedata.com/resource/pubmed/id/11879142

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0035334, umls-concept:C0037088, umls-concept:C0205314, umls-concept:C0332281, umls-concept:C0679622, umls-concept:C1417848, umls-concept:C1527180
pubmed:issue	3
pubmed:dateCreated	2002-3-6
pubmed:abstractText	To search for mutations in the neural retina leucine zipper (NRL) gene in patients with dominant retinitis pigmentosa and to compare the severity of disease in these patients with that observed previously in patients with dominant rhodopsin mutations.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/EY07076, http://linkedlifedata.com/resource/pubmed/grant/R01 EY00169, http://linkedlifedata.com/resource/pubmed/grant/R01 EY08683, http://linkedlifedata.com/resource/pubmed/grant/R01 EY11655
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7706534
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Basic-Leucine Zipper Transcription..., http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Eye Proteins, http://linkedlifedata.com/resource/pubmed/chemical/NRL protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Rhodopsin
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0003-9950
pubmed:author	pubmed-author:BersonEliot LEL, pubmed-author:DeAngelisMargaret MMM, pubmed-author:DryjaThaddeus PTP, pubmed-author:GrimsbyJonna LJL, pubmed-author:SandbergMichael AMA
pubmed:issnType	Print
pubmed:volume	120
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	369-75
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:11879142-Adult, pubmed-meshheading:11879142-Aged, pubmed-meshheading:11879142-Basic-Leucine Zipper Transcription Factors, pubmed-meshheading:11879142-Child, pubmed-meshheading:11879142-DNA Mutational Analysis, pubmed-meshheading:11879142-DNA Primers, pubmed-meshheading:11879142-DNA-Binding Proteins, pubmed-meshheading:11879142-Dark Adaptation, pubmed-meshheading:11879142-Electroretinography, pubmed-meshheading:11879142-Eye Proteins, pubmed-meshheading:11879142-Female, pubmed-meshheading:11879142-Humans, pubmed-meshheading:11879142-Leucine Zippers, pubmed-meshheading:11879142-Male, pubmed-meshheading:11879142-Mutation, Missense, pubmed-meshheading:11879142-Pedigree, pubmed-meshheading:11879142-Polymerase Chain Reaction, pubmed-meshheading:11879142-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:11879142-Retinitis Pigmentosa, pubmed-meshheading:11879142-Rhodopsin, pubmed-meshheading:11879142-Visual Acuity
pubmed:year	2002
pubmed:articleTitle	Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.
pubmed:affiliation	Massachusetts Eye and Ear Infirmary, 243 Charles St, Boston, MA 02114, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't