7987331

Source:http://linkedlifedata.com/resource/pubmed/id/7987331

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0035334, umls-concept:C0035499, umls-concept:C0205314, umls-concept:C0443147, umls-concept:C0599155, umls-concept:C0679622
pubmed:issue	8
pubmed:dateCreated	1995-1-10
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9208958
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Codon, http://linkedlifedata.com/resource/pubmed/chemical/Rhodopsin
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	0964-6906
pubmed:author	pubmed-author:BonneauDD, pubmed-author:CoscasGG, pubmed-author:DufierJ LJL, pubmed-author:GerberSS, pubmed-author:GhazeMM, pubmed-author:MunnichAA, pubmed-author:PhilipNN, pubmed-author:RozetJ MJM, pubmed-author:SoubraneGG, pubmed-author:SouiedEE
pubmed:issnType	Print
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	N
pubmed:pagination	1433-4
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:7987331-Codon, pubmed-meshheading:7987331-Genes, Dominant, pubmed-meshheading:7987331-Genotype, pubmed-meshheading:7987331-Humans, pubmed-meshheading:7987331-Point Mutation, pubmed-meshheading:7987331-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:7987331-Retinitis Pigmentosa, pubmed-meshheading:7987331-Rhodopsin
pubmed:year	1994
pubmed:articleTitle	Five novel missense mutations of the rhodopsin gene in autosomal dominant retinitis pigmentosa.
pubmed:affiliation	Service de Génétique, INSERM U-393, Hôpital des Enfants-Malades, Paris, France.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't