Direkt zum Inhalt

Owner only: item control page
Keilhauer, C. N. ; Meigen, T. ; Weber, Bernhard H. F.

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.

Date of publication of this fulltext: 07 Apr 2017 12:55
Article



Involved Institutions


Details

Item typeArticle
Journal or Publication TitleArchives of Ophthalmology
Publisher:AMER MEDICAL ASSOC
Place of Publication:CHICAGO
Volume:124
Number of Issue or Book Chapter:7
Page Range:pp. 1020-1027
Date2006
InstitutionsMedicine > Lehrstuhl für Humangenetik
Identification Number
ValueType
10.1001/archopht.124.7.1020DOI
16832026PubMed ID
KeywordsMACULAR DYSTROPHY; RETINAL DEGENERATION; RETINITIS-PIGMENTOSA; PHOTORECEPTORS; CONE; TOPOGRAPHY; OPSIN; BLUE;
Dewey Decimal Classification600 Technology > 610 Medical sciences Medicine
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgPartially
Item ID35483

Export bibliographical data

Owner only: item control page

nach oben