Hong, Hui-Mei <br/><br/>
A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss.  [electronic resource] 

 -  Human genetics  Feb 2010 
 - 191-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-1203 
<br/><br/><label>Standard No.: </label>10.1007/s00439-009-0758-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cell Membrane--metabolism<br/>Cell Survival<br/>Connexins--chemistry<br/>Endoplasmic Reticulum--metabolism<br/>Gap Junctions--metabolism<br/>Green Fluorescent Proteins--genetics<br/>HeLa Cells<br/>Hearing Loss--genetics<br/>Humans<br/>Microscopy, Fluorescence<br/>Mutant Proteins--chemistry<br/>Mutation, Missense<br/>Nerve Tissue Proteins--chemistry<br/>Protein Multimerization<br/>Recombinant Fusion Proteins--genetics<br/>Transfection