Intrafamilial phenotypic variability in families with RDS mutations: exclusion of ROM1 as a genetic modifier for those with retinitis pigmentosa. [electronic resource]
Producer: 20070130Description: 89-93 p. digitalISSN:- 0007-1161
- Adult
- Electroretinography
- Eye Proteins -- genetics
- Family Health
- Female
- Fluorescein Angiography
- Genotype
- Humans
- Intermediate Filament Proteins -- genetics
- Macular Degeneration -- genetics
- Male
- Membrane Glycoproteins -- genetics
- Membrane Proteins -- genetics
- Middle Aged
- Mutation
- Nerve Tissue Proteins -- genetics
- Pedigree
- Peripherins
- Phenotype
- Retinal Degeneration -- genetics
- Retinitis Pigmentosa -- genetics
- Tetraspanins
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Publication Type: Journal Article
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