Testa, F <br/><br/>
Clinical phenotype of an Italian family with a new mutation in the PRPF8 gene.  [electronic resource] 

 -  European journal of ophthalmology   
 - 779-81 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1120-6721 
<br/><br/><label>Standard No.: </label>10.1177/112067210601600524  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Carrier Proteins--genetics<br/>DNA--genetics<br/>Electroretinography<br/>Female<br/>Humans<br/>Italy<br/>Male<br/>Mutation<br/>Ophthalmoscopy<br/>Pedigree<br/>Phenotype<br/>RNA-Binding Proteins<br/>Retinitis Pigmentosa--diagnosis