Churchill, Jennifer D <br/><br/>
Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.  [electronic resource] 

 -  Investigative ophthalmology & visual science  Feb 2013 
 - 1411-6 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-5783 
<br/><br/><label>Standard No.: </label>10.1167/iovs.12-11541  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>DNA--genetics<br/>Electroretinography<br/>Eye Proteins--genetics<br/>Female<br/>GTP-Binding Proteins<br/>Genes, X-Linked--genetics<br/>Genetic Diseases, X-Linked--diagnosis<br/>Guanine Nucleotide Exchange Factors<br/>Humans<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Retinitis Pigmentosa--diagnosis