Genes and mutations in autosomal dominant cone and cone-rod dystrophy

Adv Exp Med Biol. 2012:723:337-43. doi: 10.1007/978-1-4614-0631-0_44.

Authors

Susanne Kohl¹, Veronique Kitiratschky, Monika Papke, Simone Schaich, Alexandra Sauer, Bernd Wissinger

Affiliation

¹ Department for Ophthalmology, Molecular Genetics Laboratory, Institute for Ophthalmic Research, University Tuebingen, Roentgenweg 11, S Tuebingen, 72076, Germany. [email protected]

PMID: 22183351
DOI: 10.1007/978-1-4614-0631-0_44

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Genes, Dominant
Genetic Predisposition to Disease / epidemiology
Genetic Predisposition to Disease / genetics
Genetic Testing
Humans
Macular Degeneration / congenital
Macular Degeneration / epidemiology*
Macular Degeneration / genetics*
Point Mutation
Prevalence
Retinal Cone Photoreceptor Cells / physiology*
Retinitis Pigmentosa / epidemiology*
Retinitis Pigmentosa / genetics*
Stargardt Disease