Clinical description and exclusion of candidate genes in a novel autosomal recessively inherited vitreoretinal dystrophy.

Sarra, Gian-Marco; Weigell-Weber, Maike; Kotzot, Dieter; Niemeyer, Gunter; Messmer, Elmar; Hergersberg, Martin

Sarra, Gian-Marco; Weigell-Weber, Maike; Kotzot, Dieter; Niemeyer, Gunter; Messmer, Elmar; Hergersberg, Martin.

Affiliation

Sarra GM; Department of Ophthalmology, University Hospital Zurich, Zurich, Switzerland.

Arch Ophthalmol ; 121(8): 1109-16, 2003 Aug.

Article in En | MEDLINE | ID: mdl-12912687

Subject(s)

Cataract/genetics; Eye Diseases, Hereditary/genetics; Genes, Recessive; Myopia/genetics; Retinal Degeneration/genetics; Vitreous Body/pathology; Aged; Atrophy; Cataract/diagnosis; Electroretinography; Eye Diseases, Hereditary/diagnosis; Female; Genetic Linkage; Genetic Markers; Humans; Male; Myopia/diagnosis; Pigment Epithelium of Eye/pathology; Polymerase Chain Reaction; Retinal Degeneration/diagnosis; Vision Disorders/genetics; Visual Field Tests; Visual Fields

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Retinal Degeneration / Vitreous Body / Cataract / Eye Diseases, Hereditary / Genes, Recessive / Myopia Type of study: Diagnostic_studies Limits: Aged / Female / Humans / Male Language: En Journal: Arch Ophthalmol Year: 2003 Document type: Article Affiliation country: Switzerland Country of publication: United States

Search on Google

Add to My VHL

XML

PubMed Links