Go to content
UR Home

Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene

Keilhauer, C N, Meigen, T and Weber, Bernhard H. F. (2006) Clinical findings in a multigeneration family with autosomal dominant central areolar choroidal dystrophy associated with an Arg195Leu mutation in the peripherin/RDS gene. Archives of Ophthalmology 124 (7), pp. 1020-1027.

Full text not available from this repository.

at publisher (via DOI)

at PubMed


Abstract

OBJECTIVE: To characterize clinical findings associated with a mutation in codon 195 (Arg195Leu) of the peripherin/RDS gene in a large multigeneration family of European decent. METHODS: Sixteen members from 2 generations underwent ophthalmologic examination, including best-corrected visual acuity, examination of the anterior segments, and inspection of the ocular fundus after pharmacologic ...

plus


Export bibliographical data



Item type:Article
Date:2006
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1001/archopht.124.7.1020DOI
16832026PubMed ID
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Partially
Item ID:35483
Owner only: item control page
  1. Homepage UR

University Library

Publication Server

Contact:

Publishing: oa@ur.de

Dissertations: dissertationen@ur.de

Research data: daten@ur.de

Contact persons