Wang, Kai Jie <br/><br/>
A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family.  [electronic resource] 

 -  Molecular vision  Jan 2011 
 - 70-7 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/>Adolescent<br/>Adult<br/>Aquaporins--genetics<br/>Cataract--congenital<br/>Child<br/>China<br/>Codon<br/>Computational Biology--methods<br/>DNA Mutational Analysis<br/>DNA Primers--genetics<br/>Eye Proteins--genetics<br/>Family Health<br/>Female<br/>Heterozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Sequence Analysis, DNA