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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
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| Item type | Article | ||||||
| Journal or Publication Title | Archives of Ophthalmology | ||||||
| Publisher: | AMER MEDICAL ASSOC | ||||||
|---|---|---|---|---|---|---|---|
| Place of Publication: | CHICAGO | ||||||
| Volume: | 124 | ||||||
| Number of Issue or Book Chapter: | 7 | ||||||
| Page Range: | pp. 1020-1027 | ||||||
| Date | 2006 | ||||||
| Institutions | Medicine > Lehrstuhl für Humangenetik | ||||||
| Identification Number |
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| Keywords | MACULAR DYSTROPHY; RETINAL DEGENERATION; RETINITIS-PIGMENTOSA; PHOTORECEPTORS; CONE; TOPOGRAPHY; OPSIN; BLUE; | ||||||
| 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 |
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