Drenth, Joost P H <br/><br/>
Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease.  [electronic resource] 

 -  Nature genetics  Mar 2003 
 - 345-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng1104  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Calcium-Binding Proteins<br/>Chromosome Mapping<br/>DNA--genetics<br/>Female<br/>Genetic Markers<br/>Germ-Line Mutation<br/>Glucosidases<br/>Haplotypes<br/>Humans<br/>Intracellular Signaling Peptides and Proteins<br/>Male<br/>Membrane Proteins<br/>Molecular Sequence Data<br/>Myristoylated Alanine-Rich C Kinase Substrate<br/>Netherlands<br/>Pedigree<br/>Phosphoproteins--genetics<br/>Polycystic Kidney, Autosomal Dominant--genetics