Chassine, Thomas <br/><br/>
Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopia.  [electronic resource] 

 -  The British journal of ophthalmology  Oct 2015 
 - 1360-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-2079 
<br/><br/><label>Standard No.: </label>10.1136/bjophthalmol-2014-306224  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>DNA--genetics<br/>DNA Mutational Analysis<br/>Electroretinography<br/>Eye Proteins--genetics<br/>Female<br/>Humans<br/>Male<br/>Microtubule-Associated Proteins<br/>Middle Aged<br/>Mutation<br/>Myopia--etiology<br/>Pedigree<br/>Phenotype<br/>Retinitis Pigmentosa--complications<br/>Visual Acuity<br/>Visual Fields<br/>Young Adult