Developments in molecular genetics and electrophysiology in inherited retinal disorders-Reference-Cited by-同舟云学术

Developments in molecular genetics and electrophysiology in inherited retinal disorders

Published:2006-03-30 Issue:2 Volume:84 Page:161-168
ISSN:1395-3907
Container-title:Acta Ophthalmologica Scandinavica
language:en
Short-container-title:

Author:

Andréasson Sten

Publisher

Wiley

Subject

Ophthalmology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0420.2006.00657.x/fullpdf

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3. Clinical expression of X-linked retinitis pigmentosa in Swedish families with mutations in the RP2 and RPGR genes;Andréasson;Ophthalmic Genet,2003

4. Electroretinographic diagnosis in families with X-linked retinitis pigmentosa;Andréasson;Acta Ophthalmol,1990

5. A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (arg-135-leu);Andréasson;Ophthalmic Paediatr Genet,1992a

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