Murphy, Daniel <br/><br/>
Alternative Splicing Shapes the Phenotype of a Mutation in BBS8 To Cause Nonsyndromic Retinitis Pigmentosa.  [electronic resource] 

 -  Molecular and cellular biology  May 2015 
 - 1860-70 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-5549 
<br/><br/><label>Standard No.: </label>10.1128/MCB.00040-15  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alternative Splicing<br/>Animals<br/>Animals, Newborn--anatomy & histology<br/>Cornea--metabolism<br/>Cytoskeletal Proteins<br/>Enhancer Elements, Genetic<br/>Exons<br/>Frameshift Mutation<br/>Mice<br/>Mice, Inbred C57BL<br/>Microtubule-Associated Proteins--genetics<br/>Organ Specificity<br/>Photoreceptor Cells--metabolism<br/>Retinitis Pigmentosa--genetics