18161623

Source:http://linkedlifedata.com/resource/pubmed/id/18161623

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0019904, umls-concept:C0026882, umls-concept:C0205082, umls-concept:C0241888, umls-concept:C0376315, umls-concept:C1314792
pubmed:issue	4
pubmed:dateCreated	2007-12-28
pubmed:abstractText	To report the clinical features of a patient with familial exudative vitreoretinopathy (FEVR) associated with homozygous R417Q mutation in the frizzled-4 gene (FZD4).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9436057
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/FZD4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Frizzled Receptors, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, G-Protein-Coupled
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1381-6810
pubmed:author	pubmed-author:HayashiKenshiK, pubmed-author:KondoHiroyukiH, pubmed-author:QinMinghuiM, pubmed-author:TahiraTomokoT, pubmed-author:UchioEiichiE
pubmed:issnType	Print
pubmed:volume	28
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	220-3
pubmed:meshHeading	pubmed-meshheading:18161623-Female, pubmed-meshheading:18161623-Frizzled Receptors, pubmed-meshheading:18161623-Homozygote, pubmed-meshheading:18161623-Humans, pubmed-meshheading:18161623-Infant, pubmed-meshheading:18161623-Mutation, pubmed-meshheading:18161623-Receptors, G-Protein-Coupled, pubmed-meshheading:18161623-Retinal Diseases, pubmed-meshheading:18161623-Suppuration, pubmed-meshheading:18161623-Vitreous Body
pubmed:year	2007
pubmed:articleTitle	Severe form of familial exudative vitreoretinopathy caused by homozygous R417Q mutation in frizzled-4 gene.
pubmed:affiliation	Department of Ophthalmology, Fukuoka University School of Medicine, Nanakuma, Jonanku, Fukuoka, Japan. hkondo@fukuoka-u.ac.up
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't