19019939

Source:http://linkedlifedata.com/resource/pubmed/id/19019939

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0035309, umls-concept:C0056207, umls-concept:C0332291, umls-concept:C0678951, umls-concept:C1567742
pubmed:issue	3
pubmed:dateCreated	2009-2-26
pubmed:abstractText	X linked Alport syndrome is characterised by renal failure, hearing loss, lenticonus, and a central and peripheral dot-and-fleck retinopathy. complement factor H (CFH) gene variants are strongly associated with retinal drusen in macular degeneration and mesangiocapillary glomerulonephritis, and this study examines their role in the development of the Alport retinopathy.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0421041
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Complement Factor H
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1468-2079
pubmed:author	pubmed-author:BairdP NPN, pubmed-author:ColvilleDD, pubmed-author:GuymerR HRH, pubmed-author:LiuJJ, pubmed-author:SavigeJJ, pubmed-author:WangY YYY
pubmed:issnType	Electronic
pubmed:volume	93
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	379-82
pubmed:meshHeading	pubmed-meshheading:19019939-Adolescent, pubmed-meshheading:19019939-Adult, pubmed-meshheading:19019939-Aged, pubmed-meshheading:19019939-Aged, 80 and over, pubmed-meshheading:19019939-Alleles, pubmed-meshheading:19019939-Child, pubmed-meshheading:19019939-Complement Factor H, pubmed-meshheading:19019939-Female, pubmed-meshheading:19019939-Genetic Predisposition to Disease, pubmed-meshheading:19019939-Haplotypes, pubmed-meshheading:19019939-Humans, pubmed-meshheading:19019939-Macular Degeneration, pubmed-meshheading:19019939-Male, pubmed-meshheading:19019939-Middle Aged, pubmed-meshheading:19019939-Nephritis, Hereditary, pubmed-meshheading:19019939-Phenotype, pubmed-meshheading:19019939-Polymorphism, Genetic, pubmed-meshheading:19019939-Retinal Degeneration, pubmed-meshheading:19019939-Retinal Drusen, pubmed-meshheading:19019939-Young Adult
pubmed:year	2009
pubmed:articleTitle	The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms.
pubmed:affiliation	The University of Melbourne, Department of Medicine (Northern Health), The Northern Hospital, Epping VIC 3076, Australia.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't