Kim, J-W <br/><br/>
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta.  [electronic resource] 

 -  Journal of medical genetics  Mar 2005 
 - 271-5 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2004.024505  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amelogenesis Imperfecta--genetics<br/>Base Sequence<br/>Child<br/>DNA Mutational Analysis<br/>Genes, Recessive<br/>Haplotypes<br/>Humans<br/>Matrix Metalloproteinase 20<br/>Matrix Metalloproteinases--chemistry<br/>Molecular Sequence Data<br/>Pedigree<br/>Phenotype