Hu, Shanshan <br/><br/>
A novel mutation in GJA8 causing congenital cataract-microcornea syndrome in a Chinese pedigree.  [electronic resource] 

 -  Molecular vision  Aug 2010 
 - 1585-92 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-0535 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Asian People--genetics<br/>Base Sequence<br/>Cataract--congenital<br/>Child<br/>Child, Preschool<br/>China<br/>Connexins--chemistry<br/>Cornea--pathology<br/>DNA Mutational Analysis<br/>Eye Proteins--chemistry<br/>Female<br/>Genes, Dominant--genetics<br/>Humans<br/>Hydrophobic and Hydrophilic Interactions<br/>Male<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Pedigree<br/>Protein Structure, Secondary<br/>Syndrome