Yasmeen, Afshan <br/><br/>
Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1.  [electronic resource] 

 -  Molecular vision  Apr 2010 
 - 682-8 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/>Base Sequence<br/>Cataract--congenital<br/>Consanguinity<br/>DNA Mutational Analysis<br/>Family<br/>Female<br/>Galactokinase--chemistry<br/>Genes, Recessive--genetics<br/>Genetic Predisposition to Disease<br/>Humans<br/>Lod Score<br/>Male<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Pakistan<br/>Pedigree<br/>Sequence Alignment