11449319

Source:http://linkedlifedata.com/resource/pubmed/id/11449319

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0030705, umls-concept:C1419391, umls-concept:C2607943, umls-concept:C2926606
pubmed:issue	2
pubmed:dateCreated	2001-7-12
pubmed:abstractText	To characterize the clinical phenotype, with emphasis on electrophysiology, of two children with suspected Bothnia dystrophy.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9436057
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/11-cis-retinal-binding protein, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1381-6810
pubmed:author	pubmed-author:AbrahamsonMM, pubmed-author:AndréassonSS, pubmed-author:GränseLL, pubmed-author:PonjavicVV
pubmed:issnType	Print
pubmed:volume	22
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	97-105
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:11449319-Carrier Proteins, pubmed-meshheading:11449319-Child, pubmed-meshheading:11449319-Dark Adaptation, pubmed-meshheading:11449319-Diagnosis, Differential, pubmed-meshheading:11449319-Electroretinography, pubmed-meshheading:11449319-Female, pubmed-meshheading:11449319-Fluorescein Angiography, pubmed-meshheading:11449319-Fundus Oculi, pubmed-meshheading:11449319-Humans, pubmed-meshheading:11449319-Image Processing, Computer-Assisted, pubmed-meshheading:11449319-Mutation, pubmed-meshheading:11449319-Phenotype, pubmed-meshheading:11449319-Photoreceptor Cells, Vertebrate, pubmed-meshheading:11449319-Polymerase Chain Reaction, pubmed-meshheading:11449319-Retinal Degeneration, pubmed-meshheading:11449319-Sensory Thresholds, pubmed-meshheading:11449319-Sweden, pubmed-meshheading:11449319-Visual Acuity, pubmed-meshheading:11449319-Visual Fields
pubmed:year	2001
pubmed:articleTitle	Electrophysiological findings in two young patients with Bothnia dystrophy and a mutation in the RLBP1 gene.
pubmed:affiliation	Department of Ophthalmology, University of Lund, Lund, Sweden. lotta.granse@brevet.nu
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't