20361016

Source:http://linkedlifedata.com/resource/pubmed/id/20361016

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015397, umls-concept:C0031809, umls-concept:C0237401, umls-concept:C0392760, umls-concept:C1522508
pubmed:dateCreated	2010-4-2
pubmed:abstractText	To determine the spectrum of mutations and phenotypic variability within patients with mutations in membrane-type frizzled related protein gene (MFRP).
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-10967077, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-11263980, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-12140190, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-15284851, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-15976030, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-17122143, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-17167404, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-17435967, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-18363166, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-18554571, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-18764959, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-19030905, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-19169412, http://linkedlifedata.com/resource/pubmed/commentcorrection/20361016-19753314
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9605351
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/MFRP protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
pubmed:status	MEDLINE
pubmed:issn	1090-0535
pubmed:author	pubmed-author:DayAlexander CAC, pubmed-author:DeverySophieS, pubmed-author:HolderGraham EGE, pubmed-author:LeroyBart PBP, pubmed-author:LiZhengZ, pubmed-author:MackayDonna SDS, pubmed-author:MukhopadhyayRajarshiR, pubmed-author:RobsonAnthony GAG, pubmed-author:SergouniotisPanagiotis IPI, pubmed-author:WebsterAndrew RAR, pubmed-author:WrightGenevieveG
pubmed:issnType	Electronic
pubmed:volume	16
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	540-8
pubmed:dateRevised	2010-9-28
pubmed:meshHeading	pubmed-meshheading:20361016-Adult, pubmed-meshheading:20361016-Base Sequence, pubmed-meshheading:20361016-Electrophysiological Phenomena, pubmed-meshheading:20361016-Electroretinography, pubmed-meshheading:20361016-Eye Diseases, pubmed-meshheading:20361016-Female, pubmed-meshheading:20361016-Fluorescence, pubmed-meshheading:20361016-Fundus Oculi, pubmed-meshheading:20361016-Humans, pubmed-meshheading:20361016-Male, pubmed-meshheading:20361016-Membrane Proteins, pubmed-meshheading:20361016-Middle Aged, pubmed-meshheading:20361016-Molecular Sequence Data, pubmed-meshheading:20361016-Mutation, pubmed-meshheading:20361016-Pedigree, pubmed-meshheading:20361016-Phenotype, pubmed-meshheading:20361016-Tomography, Optical Coherence
pubmed:year	2010
pubmed:articleTitle	A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy.
pubmed:affiliation	Department of Genetics, Institute of Ophthalmology, University College London, UK. docrajarshi@doctors.org.uk
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't