Huang, Y <br/><br/>
A novel deletion mutation in RS1 gene caused X-linked juvenile retinoschisis in a Chinese family.  [electronic resource] 

 -  Eye (London, England)  Nov 2014 
 - 1364-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5454 
<br/><br/><label>Standard No.: </label>10.1038/eye.2014.196  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asian People--genetics<br/>Base Sequence<br/>Child<br/>China<br/>DNA Mutational Analysis<br/>Eye Proteins--genetics<br/>Fluorescein Angiography<br/>Frameshift Mutation<br/>Humans<br/>Infant<br/>Male<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Retinoschisis--genetics<br/>Sequence Deletion<br/>Tomography, Optical Coherence<br/>Visual Acuity