Chen, Xuejuan <br/><br/>
Targeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseases.  [electronic resource] 

 -  Investigative ophthalmology & visual science  Mar 2013 
 - 2186-97 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-5783 
<br/><br/><label>Standard No.: </label>10.1167/iovs.12-10967  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asian People--genetics<br/>China<br/>Cohort Studies<br/>DNA Mutational Analysis--methods<br/>Genetic Predisposition to Disease<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Microarray Analysis<br/>Mutation--genetics<br/>Pedigree<br/>Retinal Dystrophies--congenital