Leroy, B P <br/><br/>
Intrafamilial phenotypic variability in families with RDS mutations: exclusion of ROM1 as a genetic modifier for those with retinitis pigmentosa.  [electronic resource] 

 -  The British journal of ophthalmology  Jan 2007 
 - 89-93 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0007-1161 
<br/><br/><label>Standard No.: </label>10.1136/bjo.2006.101915  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Electroretinography<br/>Eye Proteins--genetics<br/>Family Health<br/>Female<br/>Fluorescein Angiography<br/>Genotype<br/>Humans<br/>Intermediate Filament Proteins--genetics<br/>Macular Degeneration--genetics<br/>Male<br/>Membrane Glycoproteins--genetics<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Pedigree<br/>Peripherins<br/>Phenotype<br/>Retinal Degeneration--genetics<br/>Retinitis Pigmentosa--genetics<br/>Tetraspanins