Chen, Ying-Ting <br/><br/>
Novel mutations in the helix termination motif of keratin 3 and keratin 12 in 2 Taiwanese families with Meesmann corneal dystrophy.  [electronic resource] 

 -  Cornea  Nov 2005 
 - 928-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0277-3740 
<br/><br/><label>Standard No.: </label>10.1097/01.ico.0000159732.29930.26  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Cornea--pathology<br/>Corneal Dystrophies, Hereditary--ethnology<br/>DNA--genetics<br/>Exons<br/>Genotype<br/>Heterozygote<br/>Humans<br/>Keratin-12<br/>Keratin-3<br/>Keratins--genetics<br/>Male<br/>Mutation, Missense<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Taiwan